rs786205093(C;C)

common in clinvar

Is a	genotype
of	rs786205093
Gene	PRF1
Chromosome	10
Position	70,600,696
mentioned	by

Magnitude

0

Repute

Good

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