rs397507961

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 rs397507961(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32363266

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507961
dbSNP (classic)	rs397507961
ClinGen	rs397507961
ebi	rs397507961
HLI	rs397507961
Exac	rs397507961
Gnomad	rs397507961
Varsome	rs397507961
LitVar	rs397507961
Map	rs397507961
PheGenI	rs397507961
Biobank	rs397507961
1000 genomes	rs397507961
hgdp	rs397507961
ensembl	rs397507961
geneview	rs397507961
scholar	rs397507961
google	rs397507961
pharmgkb	rs397507961
gwascentral	rs397507961
openSNP	rs397507961
23andMe	rs397507961
SNPshot	rs397507961
SNPdbe	rs397507961
MSV3d	rs397507961
GWAS Ctlg	rs397507961

Max Magnitude

6

ClinVar
Risk	rs397507961(-;-)
Alt	rs397507961(-;-)
Reference	Rs397507961(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.32937403_32937404delCT
CLNSRC	ClinVar
CLNACC	RCV000045409.2, RCV000256904.2,