| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs61748436 |
G>A |
Pathogenic, likely-pathogenic |
Coding sequence variant, missense variant |
|
rs61748449 |
G>- |
Not-provided, pathogenic |
Coding sequence variant, frameshift variant |
|
rs62654391 |
G>A |
Not-provided, likely-pathogenic |
Coding sequence variant, missense variant |
|
rs104894671 |
A>C |
Not-provided, pathogenic |
Coding sequence variant, missense variant |
|
rs104894672 |
C>T |
Not-provided, pathogenic |
Coding sequence variant, missense variant |
|
rs104894673 |
C>T |
Not-provided, pathogenic |
Coding sequence variant, missense variant |
|
rs139340178 |
C>G |
Uncertain-significance, likely-benign, conflicting-interpretations-of-pathogenicity |
Missense variant, coding sequence variant |
|
rs281865198 |
T>C |
Likely-pathogenic |
Splice donor variant |
|
rs281865515 |
G>- |
Pathogenic, not-provided |
Coding sequence variant, frameshift variant |
|
rs281865516 |
C>- |
Pathogenic, not-provided |
Coding sequence variant, frameshift variant |
|
rs527236062 |
G>C |
Pathogenic |
Coding sequence variant, missense variant |
|
rs527236063 |
G>A,C |
Likely-pathogenic |
Coding sequence variant, missense variant, synonymous variant |
|
rs756105390 |
G>A,C |
Likely-pathogenic |
Synonymous variant, coding sequence variant, missense variant |
|
rs771450991 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs786205521 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs786205630 |
C>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs863224863 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs864309706 |
C>G |
Pathogenic |
Coding sequence variant, stop gained |
|
rs864309707 |
C>- |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs864309708 |
T>- |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs869312175 |
C>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs878853383 |
G>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs886044121 |
T>- |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs1064796109 |
GAG>TTA |
Likely-pathogenic |
Intron variant |
|
rs1064797246 |
C>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs1064797247 |
C>A |
Likely-pathogenic |
Coding sequence variant, stop gained |
|
rs1437021651 |
C>T |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1555801777 |
->A |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1555801963 |
C>T |
Likely-pathogenic |
Coding sequence variant, stop gained |
|
rs1555801989 |
TC>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1555802058 |
CTGGACTACA>GATCCC |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1568626209 |
G>- |
Pathogenic |
Frameshift variant, coding sequence variant |
|
rs1568626289 |
G>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1599991268 |
->C |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1599991538 |
GT>- |
Likely-pathogenic |
Frameshift variant, coding sequence variant |
|
rs1599991611 |
CA>- |
Pathogenic |
Stop gained, coding sequence variant |
|
rs1599992622 |
G>A |
Likely-pathogenic |
Stop gained, coding sequence variant |
|
rs1599992745 |
T>C |
Likely-pathogenic |
Terminator codon variant, stop lost |