rs397507743

Orientation

plus

Stabilized

plus

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

Make rs397507743(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339163

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507743
dbSNP (classic)	rs397507743
ClinGen	rs397507743
ebi	rs397507743
HLI	rs397507743
Exac	rs397507743
Gnomad	rs397507743
Varsome	rs397507743
LitVar	rs397507743
Map	rs397507743
PheGenI	rs397507743
Biobank	rs397507743
1000 genomes	rs397507743
hgdp	rs397507743
ensembl	rs397507743
geneview	rs397507743
scholar	rs397507743
google	rs397507743
pharmgkb	rs397507743
gwascentral	rs397507743
openSNP	rs397507743
23andMe	rs397507743
SNPshot	rs397507743
SNPdbe	rs397507743
MSV3d	rs397507743
GWAS Ctlg	rs397507743

Max Magnitude

6

ClinVar
Risk	rs397507743(-;-)
Alt	rs397507743(-;-)
Reference	Rs397507743(A;A)
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.32913300delA
CLNSRC	ClinVar
CLNACC	RCV000044496.2, RCV000256507.2,