rs104893831(G;G)

common in clinvar

Is a	genotype
of	rs104893831
Gene	VHL
Chromosome	3
Position	10,146,549
mentioned	by

Magnitude

0

Repute

Good

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