rs747169857(G;G)

common in clinvar

Is a	genotype
of	rs747169857
Gene	UNC13D
Chromosome	17
Position	75,840,050
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