rs766657895(G;G)

common in clinvar

Is a	genotype
of	rs766657895
Gene	UNC13D
Chromosome	17
Position	75,830,592
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