rs606231403

Merged into

rs80359548

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar

Make rs606231403(-;T)

Make rs606231403(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32340286

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs606231403
dbSNP (classic)	rs606231403
ClinGen	rs606231403
ebi	rs606231403
HLI	rs606231403
Exac	rs606231403
Gnomad	rs606231403
Varsome	rs606231403
LitVar	rs606231403
Map	rs606231403
PheGenI	rs606231403
Biobank	rs606231403
1000 genomes	rs606231403
hgdp	rs606231403
ensembl	rs606231403
geneview	rs606231403
scholar	rs606231403
google	rs606231403
pharmgkb	rs606231403
gwascentral	rs606231403
openSNP	rs606231403
23andMe	rs606231403
SNPshot	rs606231403
SNPdbe	rs606231403
MSV3d	rs606231403
GWAS Ctlg	rs606231403

Status

Merged into rs80359548

Max Magnitude

0

ClinVar
Risk	rs606231403(T;T)
Alt	rs606231403(T;T)
Reference	Rs606231403(;)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32914426dupT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000113505.3, RCV000164167.1,