rs28897759(A;A)

common in complete genomics

Is a	genotype
of	rs28897759
Gene	BRCA2
Chromosome	13
Position	32,394,803
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(A;A)	0	common in complete genomics
(A;T)	5.5	BRCA2 variant, possibly causal mutation but not definite