rs104894182(G;G)

common in clinvar

Is a	genotype
of	rs104894182
Gene	PRF1
Chromosome	10
Position	70,598,885
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