rs61736587(G;G)

common in clinvar

Is a	genotype
of	rs61736587
Gene	STXBP2
Chromosome	19
Position	7,647,436
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;G)	3	Carrier of a hemophagocytic lymphohistiocytosis (HLH) mutation
(G;G)	0	common in clinvar