SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs61884288 |
G>A |
Benign, pathogenic, likely-benign |
Coding sequence variant, missense variant, non coding transcript variant |
rs113304476 |
T>C |
Pathogenic |
Intron variant |
rs200449378 |
T>A,C |
Pathogenic |
Intron variant |
rs281865101 |
->G |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
rs281865102 |
A>C |
Pathogenic |
Non coding transcript variant, coding sequence variant, intron variant, missense variant |
rs281865103 |
CTAA>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, intron variant, frameshift variant |
rs281865104 |
G>A |
Pathogenic |
Non coding transcript variant, coding sequence variant, stop gained |
rs281865105 |
A>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
rs397507169 |
->TC |
Pathogenic |
Coding sequence variant, frameshift variant, non coding transcript variant |
rs753928208 |
GAG>- |
Pathogenic |
Inframe deletion, coding sequence variant, non coding transcript variant |
rs755827664 |
C>- |
Pathogenic |
Coding sequence variant, frameshift variant, non coding transcript variant |
rs764296457 |
C>G,T |
Pathogenic |
Missense variant, coding sequence variant, non coding transcript variant |
rs766602179 |
G>- |
Likely-pathogenic, uncertain-significance |
Coding sequence variant, non coding transcript variant, frameshift variant |
rs779921624 |
G>A,C,T |
Likely-pathogenic |
Missense variant, stop gained, non coding transcript variant, coding sequence variant, intron variant |
rs886041723 |
AACA>- |
Pathogenic |
Frameshift variant, non coding transcript variant, coding sequence variant, intron variant |
rs1131692146 |
C>- |
Pathogenic |
Non coding transcript variant, intron variant, coding sequence variant, frameshift variant |
rs1131692147 |
GAGAG>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
rs1131692148 |
G>A |
Pathogenic |
Non coding transcript variant, stop gained, coding sequence variant |
rs1131692149 |
A>G |
Pathogenic |
Non coding transcript variant, intron variant, coding sequence variant, missense variant |
rs1131692150 |
C>T |
Pathogenic |
Intron variant, synonymous variant, non coding transcript variant, 5 prime UTR variant, coding sequence variant |
rs1131692151 |
CT>- |
Pathogenic |
Non coding transcript variant, coding sequence variant, frameshift variant |
rs1554948134 |
T>- |
Pathogenic |
Coding sequence variant, non coding transcript variant, frameshift variant, intron variant |
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