| SNP ID |
Visualize variation |
Clinical significance |
Consequence |
|
rs28934897 |
G>A |
Pathogenic, uncertain-significance |
Missense variant, genic downstream transcript variant, coding sequence variant |
|
rs72648042 |
C>T |
Conflicting-interpretations-of-pathogenicity |
Genic downstream transcript variant, synonymous variant, coding sequence variant |
|
rs76914224 |
G>A |
Conflicting-interpretations-of-pathogenicity, likely-benign, not-provided |
Coding sequence variant, missense variant |
|
rs104895298 |
G>A |
Pathogenic, not-provided |
Coding sequence variant, intron variant, missense variant |
|
rs104895300 |
C>T |
Pathogenic, likely-pathogenic |
Coding sequence variant, intron variant, missense variant |
|
rs104895301 |
G>A |
Pathogenic |
Coding sequence variant, missense variant |
|
rs104895304 |
T>C |
Pathogenic |
Coding sequence variant, missense variant |
|
rs104895311 |
G>A |
Pathogenic, not-provided |
Coding sequence variant, stop gained |
|
rs104895317 |
G>A |
Pathogenic |
Coding sequence variant, genic downstream transcript variant, missense variant |
|
rs104895319 |
G>A |
Pathogenic, not-provided |
Coding sequence variant, genic downstream transcript variant, missense variant |
|
rs104895323 |
G>-,GG |
Pathogenic, not-provided |
Frameshift variant, coding sequence variant, intron variant |
|
rs104895324 |
A>G |
Likely-pathogenic, not-provided, uncertain-significance |
Coding sequence variant, genic downstream transcript variant, missense variant |
|
rs104895332 |
T>C |
Likely-pathogenic, pathogenic, not-provided |
Coding sequence variant, missense variant |
|
rs104895352 |
G>A |
Pathogenic, not-provided |
Coding sequence variant, missense variant |
|
rs104895360 |
C>T |
Pathogenic, not-provided |
Coding sequence variant, stop gained, genic downstream transcript variant |
|
rs104895362 |
G>A,T |
Pathogenic, not-provided |
Splice donor variant, genic downstream transcript variant |
|
rs104895366 |
A>T |
Pathogenic, not-provided |
Coding sequence variant, missense variant |
|
rs104895373 |
->C |
Pathogenic, not-provided |
Frameshift variant, coding sequence variant, intron variant |
|
rs104895382 |
T>C |
Likely-pathogenic, pathogenic, not-provided |
Coding sequence variant, missense variant |
|
rs121917789 |
A>C,G |
Pathogenic |
Coding sequence variant, genic downstream transcript variant, missense variant |
|
rs121917790 |
C>T |
Pathogenic |
Coding sequence variant, intron variant, missense variant |
|
rs138342076 |
C>T |
Conflicting-interpretations-of-pathogenicity, benign |
Coding sequence variant, intron variant, synonymous variant |
|
rs397514570 |
T>C |
Pathogenic |
Missense variant, coding sequence variant |
|
rs397514571 |
T>C |
Pathogenic |
Missense variant, coding sequence variant |
|
rs398122910 |
T>C |
Pathogenic |
Splice donor variant, genic downstream transcript variant |
|
rs398122911 |
T>C |
Pathogenic |
Genic downstream transcript variant, missense variant, coding sequence variant |
|
rs758026399 |
C>T |
Pathogenic |
Stop gained, coding sequence variant |
|
rs759997079 |
A>G |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs775474803 |
C>G,T |
Pathogenic |
Intron variant, missense variant, coding sequence variant |
|
rs886048933 |
C>T |
Uncertain-significance, likely-pathogenic |
Coding sequence variant, genic downstream transcript variant, stop gained |
|
rs1295630463 |
A>G,T |
Likely-pathogenic |
Intron variant |
|
rs1555278380 |
G>A |
Likely-pathogenic |
Missense variant, coding sequence variant |
|
rs1555279757 |
T>C |
Likely-pathogenic |
Stop lost, terminator codon variant, genic downstream transcript variant |
|
rs1566147222 |
T>A |
Pathogenic |
Stop gained, coding sequence variant |
|
rs1593015642 |
CT>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |
|
rs1593021917 |
G>A |
Pathogenic |
Stop gained, coding sequence variant |
|
rs1593026935 |
TC>- |
Likely-pathogenic |
Coding sequence variant, frameshift variant |