rs398123011(G;G)

common in clinvar

Is a	genotype
of	rs398123011
Gene	SNX10
Chromosome	7
Position	26,364,575
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;A)	5.8	Osteopetrosis, type 8
(A;G)	3	Carrier of a pathogenic mutation for osteopetrosis
(G;G)	0	common in clinvar