rs180177115(C;T)

Clinical significance is uncertain (wrt breast cancer) according to ClinVar

Is a	genotype
of	rs180177115
Gene	PALB2
Chromosome	16
Position	23,629,231
mentioned	by

Magnitude

2

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	2	Clinical significance is uncertain (wrt breast cancer) according to ClinVar
(T;T)	2	Clinical significance is uncertain wrt breast cancer, according to ClinVar