rs104893826(G;G)

common in clinvar

Is a	genotype
of	rs104893826
Gene	VHL
Chromosome	3
Position	10,142,038
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;G)	7	Von Hippel-Lindau syndrome mutation
(G;G)	0	common in clinvar