rs606231396

Merged into

rs80359288

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;G)	6	BRCA2 variant considered pathogenic for breast cancer

Make rs606231396(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32333020

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs606231396
dbSNP (classic)	rs606231396
ClinGen	rs606231396
ebi	rs606231396
HLI	rs606231396
Exac	rs606231396
Gnomad	rs606231396
Varsome	rs606231396
LitVar	rs606231396
Map	rs606231396
PheGenI	rs606231396
Biobank	rs606231396
1000 genomes	rs606231396
hgdp	rs606231396
ensembl	rs606231396
geneview	rs606231396
scholar	rs606231396
google	rs606231396
pharmgkb	rs606231396
gwascentral	rs606231396
openSNP	rs606231396
23andMe	rs606231396
SNPshot	rs606231396
SNPdbe	rs606231396
MSV3d	rs606231396
GWAS Ctlg	rs606231396

Status

Merged into rs80359288

Max Magnitude

6

rs606231396 has merged into rs80359288

ClinVar
Risk	rs606231396(G;G)
Alt	rs606231396(G;G)
Reference	Rs606231396(;)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32907157dupG
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000112932.2,