rs397507815

Merged into

rs80359551

Orientation

plus

Stabilized

plus

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

Make rs397507815(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340309

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507815
dbSNP (classic)	rs397507815
ClinGen	rs397507815
ebi	rs397507815
HLI	rs397507815
Exac	rs397507815
Gnomad	rs397507815
Varsome	rs397507815
LitVar	rs397507815
Map	rs397507815
PheGenI	rs397507815
Biobank	rs397507815
1000 genomes	rs397507815
hgdp	rs397507815
ensembl	rs397507815
geneview	rs397507815
scholar	rs397507815
google	rs397507815
pharmgkb	rs397507815
gwascentral	rs397507815
openSNP	rs397507815
23andMe	rs397507815
SNPshot	rs397507815
SNPdbe	rs397507815
MSV3d	rs397507815
GWAS Ctlg	rs397507815

Status

Merged into rs80359551

Max Magnitude

6

ClinVar
Risk
Alt
Reference	Rs397507815(TC;TC)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32914446_32914447delCT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000044802.2, RCV000113509.2,