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rs745452577(G;G)

From SNPedia

common in clinvar
Is agenotype
ofrs745452577
GeneHSPG2
Chromosome1
Position21,865,798
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 1 Of uncertain significance relative to Schwartz Jampel syndrome according to ClinVar
(G;G) 0 common in clinvar