rs587776852(G;G)

common in clinvar

Is a	genotype
of	rs587776852
Gene	APOB
Chromosome	2
Position	21,005,156
mentioned	by

Magnitude

0

Repute

Good

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