rs397507781

Orientation

plus

Stabilized

plus

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

Make rs397507781(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339710

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507781
dbSNP (classic)	rs397507781
ClinGen	rs397507781
ebi	rs397507781
HLI	rs397507781
Exac	rs397507781
Gnomad	rs397507781
Varsome	rs397507781
LitVar	rs397507781
Map	rs397507781
PheGenI	rs397507781
Biobank	rs397507781
1000 genomes	rs397507781
hgdp	rs397507781
ensembl	rs397507781
geneview	rs397507781
scholar	rs397507781
google	rs397507781
pharmgkb	rs397507781
gwascentral	rs397507781
openSNP	rs397507781
23andMe	rs397507781
SNPshot	rs397507781
SNPdbe	rs397507781
MSV3d	rs397507781
GWAS Ctlg	rs397507781

Max Magnitude

6

ClinVar
Risk	rs397507781(T;T)
Alt	rs397507781(T;T)
Reference	Rs397507781(-;-)
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.32913847dupT
CLNSRC	ClinVar
CLNACC	RCV000044644.2, RCV000257094.2,