rs121918391(T;T)

common in clinvar

Is a	genotype
of	rs121918391
Gene	APOB
Chromosome	2
Position	21,015,169
mentioned	by

Magnitude

0

Repute

Good

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