rs397507933

Orientation

plus

Stabilized

plus

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

Make rs397507933(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32357805

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507933
dbSNP (classic)	rs397507933
ClinGen	rs397507933
ebi	rs397507933
HLI	rs397507933
Exac	rs397507933
Gnomad	rs397507933
Varsome	rs397507933
LitVar	rs397507933
Map	rs397507933
PheGenI	rs397507933
Biobank	rs397507933
1000 genomes	rs397507933
hgdp	rs397507933
ensembl	rs397507933
geneview	rs397507933
scholar	rs397507933
google	rs397507933
pharmgkb	rs397507933
gwascentral	rs397507933
openSNP	rs397507933
23andMe	rs397507933
SNPshot	rs397507933
SNPdbe	rs397507933
MSV3d	rs397507933
GWAS Ctlg	rs397507933

Max Magnitude

6

ClinVar
Risk	rs397507933(T;T)
Alt	rs397507933(T;T)
Reference	Rs397507933(-;-)
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.32931942_32931943insT
CLNSRC	ClinVar
CLNACC	RCV000045287.2, RCV000257502.2,