Have questions? Visit https://www.reddit.com/r/SNPedia

rs137853248(G;G)

From SNPedia

common in clinvar
Is agenotype
ofrs137853248
GeneHSPG2
Chromosome1
Position21,864,874
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 7.8 Schwartz Jampel syndrome type 1
(A;G) 3 Carrier for a Schwartz Jampel syndrome mutation
(G;G) 0 common in clinvar