rs397507646

Orientation

plus

Stabilized

plus

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

Make rs397507646(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32319298

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507646
dbSNP (classic)	rs397507646
ClinGen	rs397507646
ebi	rs397507646
HLI	rs397507646
Exac	rs397507646
Gnomad	rs397507646
Varsome	rs397507646
LitVar	rs397507646
Map	rs397507646
PheGenI	rs397507646
Biobank	rs397507646
1000 genomes	rs397507646
hgdp	rs397507646
ensembl	rs397507646
geneview	rs397507646
scholar	rs397507646
google	rs397507646
pharmgkb	rs397507646
gwascentral	rs397507646
openSNP	rs397507646
23andMe	rs397507646
SNPshot	rs397507646
SNPdbe	rs397507646
MSV3d	rs397507646
GWAS Ctlg	rs397507646

Max Magnitude

6

ClinVar
Risk	rs397507646(T;T)
Alt	rs397507646(T;T)
Reference	Rs397507646(G;G)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000013.10:g.32893435G>T
CLNSRC	ClinVar
CLNACC	RCV000044083.2, RCV000083095.4, RCV000166898.1, RCV000214710.1,