rs606231399

Merged into

rs80359335

Orientation

plus

Stabilized

plus

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

Make rs606231399(-;A)

Make rs606231399(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32336938

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs606231399
dbSNP (classic)	rs606231399
ClinGen	rs606231399
ebi	rs606231399
HLI	rs606231399
Exac	rs606231399
Gnomad	rs606231399
Varsome	rs606231399
LitVar	rs606231399
Map	rs606231399
PheGenI	rs606231399
Biobank	rs606231399
1000 genomes	rs606231399
hgdp	rs606231399
ensembl	rs606231399
geneview	rs606231399
scholar	rs606231399
google	rs606231399
pharmgkb	rs606231399
gwascentral	rs606231399
openSNP	rs606231399
23andMe	rs606231399
SNPshot	rs606231399
SNPdbe	rs606231399
MSV3d	rs606231399
GWAS Ctlg	rs606231399

Status

Merged into rs80359335

Max Magnitude

0

ClinVar
Risk	rs606231399(A;A)
Alt	rs606231399(A;A)
Reference	Rs606231399(;)
Significance	Pathogenic
Disease	Breast-ovarian cancer Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2 Hereditary breast and ovarian cancer syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32911080dupA
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000031374.10, RCV000044019.3, RCV000218358.1,