rs387906569(G;G)

common in clinvar

Is a	genotype
of	rs387906569
Gene	APOB
Chromosome	2
Position	21,004,451
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(-;G)	3	Carrier of a hypobetalipoproteinemia mutation
(G;G)	0	common in clinvar