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rs61736587(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs61736587
GeneSTXBP2
Chromosome19
Position7,647,436
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 3 Carrier of a hemophagocytic lymphohistiocytosis (HLH) mutation
(G;G) 0 common in clinvar