| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs137852695 |
T>A |
Pathogenic |
Missense variant, intron variant, coding sequence variant |
|
rs137852696 |
T>G |
Pathogenic |
Missense variant, intron variant, coding sequence variant |
|
rs137852697 |
T>C |
Pathogenic |
Missense variant, intron variant, coding sequence variant |
|
rs137852698 |
A>T |
Pathogenic |
Missense variant, coding sequence variant |
|
rs137852699 |
A>T |
Pathogenic-likely-pathogenic, pathogenic |
Stop gained, coding sequence variant |
|
rs137852700 |
G>A,C |
Pathogenic-likely-pathogenic, pathogenic |
Stop gained, missense variant, coding sequence variant |
|
rs137852701 |
C>G |
Pathogenic |
Missense variant, intron variant, coding sequence variant |
|
rs137852702 |
C>T |
Pathogenic |
Missense variant, intron variant, coding sequence variant |
|
rs143657539 |
C>T |
Pathogenic |
Intron variant, coding sequence variant, missense variant |
|
rs148412181 |
C>A,T |
Likely-pathogenic, pathogenic-likely-pathogenic |
Missense variant, coding sequence variant |
|
rs371213189 |
C>G,T |
Conflicting-interpretations-of-pathogenicity, likely-benign |
Coding sequence variant, synonymous variant |
|
rs386833624 |
TGAT>- |
Likely-pathogenic |
3 prime UTR variant |
|
rs386833625 |
C>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs386833626 |
C>A,T |
Likely-pathogenic |
Coding sequence variant, missense variant, stop gained |
|
rs386833627 |
A>T |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs386833628 |
C>T |
Likely-pathogenic |
Splice donor variant |
|
rs386833629 |
A>C |
Likely-pathogenic |
Intron variant |
|
rs386833630 |
T>C |
Likely-pathogenic |
Splice acceptor variant, intron variant |
|
rs386833631 |
C>T |
Likely-pathogenic |
Coding sequence variant, missense variant, intron variant |
|
rs386833632 |
->ACA |
Likely-pathogenic |
Inframe insertion, coding sequence variant, intron variant |
|
rs386833633 |
T>A |
Likely-pathogenic |
Coding sequence variant, stop gained, intron variant |
|
rs386833634 |
->T |
Pathogenic, pathogenic-likely-pathogenic |
Coding sequence variant, frameshift variant, intron variant |
|
rs386833635 |
C>- |
Pathogenic |
Coding sequence variant, frameshift variant, intron variant |
|
rs386833636 |
A>G |
Likely-pathogenic |
Intron variant |
|
rs386833637 |
AAG>- |
Likely-pathogenic |
Coding sequence variant, inframe deletion, intron variant |
|
rs386833638 |
CACACTGTTGTTACTTG>AA |
Likely-pathogenic |
Coding sequence variant, intron variant, inframe indel |
|
rs386833641 |
T>A,C |
Likely-pathogenic, uncertain-significance, likely-benign |
Coding sequence variant, missense variant, stop gained, intron variant |
|
rs386833642 |
A>C |
Pathogenic, likely-pathogenic |
Coding sequence variant, missense variant, intron variant |
|
rs386833643 |
A>C |
Likely-pathogenic |
Intron variant |
|
rs386833644 |
A>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant, intron variant |
|
rs386833645 |
C>T |
Likely-pathogenic |
Initiator codon variant, missense variant |
|
rs386833647 |
C>T |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs386833648 |
G>A,T |
Likely-pathogenic |
Synonymous variant, coding sequence variant, stop gained |
|
rs386833649 |
G>A |
Pathogenic-likely-pathogenic |
Coding sequence variant, stop gained |
|
rs386833650 |
G>A,C |
Pathogenic, pathogenic-likely-pathogenic, likely-pathogenic |
Coding sequence variant, missense variant, stop gained |
|
rs386833651 |
C>T |
Pathogenic, likely-pathogenic |
Splice donor variant |
|
rs386833652 |
A>G |
Likely-pathogenic |
Splice donor variant |
|
rs386833653 |
->G |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs386833654 |
G>A |
Likely-pathogenic |
Coding sequence variant, stop gained |
|
rs386833655 |
C>T |
Pathogenic, likely-pathogenic |
Coding sequence variant, missense variant |
|
rs386833656 |
C>T |
Likely-pathogenic |
Coding sequence variant, stop gained |
|
rs386833657 |
T>C |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs386833658 |
G>A,C |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs386833659 |
C>A,T |
Pathogenic, likely-pathogenic |
Splice acceptor variant |
|
rs386833660 |
T>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs386833661 |
A>G |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs386833662 |
A>G |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs386833663 |
A>C |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs386833664 |
T>A |
Pathogenic-likely-pathogenic, likely-pathogenic |
Splice acceptor variant, intron variant |
|
rs386833665 |
A>G |
Likely-pathogenic |
Coding sequence variant, missense variant, intron variant |
|
rs386833666 |
C>A,T |
Likely-pathogenic |
Coding sequence variant, missense variant, intron variant |
|
rs386833667 |
->T |
Likely-pathogenic |
Coding sequence variant, frameshift variant, intron variant |
|
rs386833668 |
G>A |
Likely-pathogenic |
Coding sequence variant, stop gained |
|
rs386833669 |
A>G |
Likely-pathogenic |
Coding sequence variant, missense variant |
|
rs386833670 |
C>T |
Likely-pathogenic |
Coding sequence variant, stop gained |
|
rs386833671 |
A>C,G |
Likely-pathogenic, uncertain-significance |
Coding sequence variant, missense variant |
|
rs560471003 |
G>A,T |
Uncertain-significance, conflicting-interpretations-of-pathogenicity |
Coding sequence variant, missense variant |
|
rs747204624 |
G>A,T |
Likely-pathogenic |
Stop gained, coding sequence variant, missense variant |
|
rs762226836 |
CCAAGAGCCACAG>-,CCAAGAGCCACAGCCAAGAGCCACAG |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs764051026 |
T>C |
Likely-pathogenic |
Intron variant, coding sequence variant, missense variant |
|
rs794727955 |
C>- |
Pathogenic |
Coding sequence variant, frameshift variant |
|
rs796052923 |
C>T |
Pathogenic |
Splice donor variant, intron variant |
|
rs796052924 |
C>T |
Pathogenic |
Intron variant |
|
rs796052925 |
G>A |
Pathogenic, likely-pathogenic |
Coding sequence variant, intron variant, stop gained |
|
rs796052927 |
A>G |
Pathogenic, likely-pathogenic |
Missense variant, initiator codon variant |
|
rs878853322 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs878853323 |
A>G |
Likely-pathogenic |
Missense variant, coding sequence variant, intron variant |
|
rs878853324 |
A>T |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs878853325 |
C>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs878853929 |
C>A |
Likely-pathogenic |
Splice donor variant, intron variant |
|
rs886041568 |
C>- |
Pathogenic, likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1057516447 |
G>T |
Likely-pathogenic |
Stop gained, intron variant, coding sequence variant |
|
rs1057516575 |
->A |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs1057516889 |
->T |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs1057517049 |
->AAGT |
Likely-pathogenic |
Intron variant, coding sequence variant, frameshift variant |
|
rs1057517112 |
TCCATGG>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs1057517192 |
T>- |
Likely-pathogenic |
Intron variant, coding sequence variant, frameshift variant |
|
rs1057517368 |
A>T |
Likely-pathogenic |
Splice donor variant |
|
rs1057517401 |
C>T |
Likely-pathogenic |
Splice donor variant, intron variant |
|
rs1085307087 |
T>C |
Likely-pathogenic |
Initiator codon variant, missense variant |
|
rs1265044710 |
C>A |
Likely-pathogenic |
Splice donor variant |
|
rs1302326945 |
->AC |
Pathogenic |
Coding sequence variant, frameshift variant |
|
rs1349528345 |
->T |
Likely-pathogenic |
Coding sequence variant, intron variant, frameshift variant |
|
rs1553166135 |
G>A |
Likely-pathogenic |
Coding sequence variant, stop gained |
|
rs1553166147 |
T>C |
Likely-pathogenic |
Splice acceptor variant |
|
rs1553166337 |
A>G |
Likely-pathogenic |
Intron variant, splice donor variant |
|
rs1553166499 |
A>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1553167415 |
C>T |
Likely-pathogenic |
Intron variant, splice donor variant |
|
rs1553167430 |
T>C |
Likely-pathogenic |
Intron variant, splice acceptor variant |
|
rs1553167474 |
C>- |
Likely-pathogenic |
Intron variant, frameshift variant, coding sequence variant |
|
rs1553167479 |
GT>- |
Likely-pathogenic |
Intron variant, frameshift variant, coding sequence variant |
|
rs1553167863 |
GCAG>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1557714302 |
A>C |
Likely-pathogenic |
Intron variant, stop gained, coding sequence variant |
|
rs1570467252 |
A>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1570470281 |
CA>- |
Pathogenic |
Intron variant, frameshift variant, coding sequence variant |
|
rs1570476221 |
C>- |
Pathogenic |
Frameshift variant, coding sequence variant |