rs397507988

Orientation

plus

Stabilized

plus

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

Make rs397507988(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32370533

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507988
dbSNP (classic)	rs397507988
ClinGen	rs397507988
ebi	rs397507988
HLI	rs397507988
Exac	rs397507988
Gnomad	rs397507988
Varsome	rs397507988
LitVar	rs397507988
Map	rs397507988
PheGenI	rs397507988
Biobank	rs397507988
1000 genomes	rs397507988
hgdp	rs397507988
ensembl	rs397507988
geneview	rs397507988
scholar	rs397507988
google	rs397507988
pharmgkb	rs397507988
gwascentral	rs397507988
openSNP	rs397507988
23andMe	rs397507988
SNPshot	rs397507988
SNPdbe	rs397507988
MSV3d	rs397507988
GWAS Ctlg	rs397507988

Max Magnitude

6

ClinVar
Risk	rs397507988(T;T)
Alt	rs397507988(T;T)
Reference	Rs397507988(-;-)
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.32944670dupT
CLNSRC	ClinVar
CLNACC	RCV000045527.2, RCV000241216.2,