rs397507703

Orientation

plus

Stabilized

plus

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

Make rs397507703(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338450

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507703
dbSNP (classic)	rs397507703
ClinGen	rs397507703
ebi	rs397507703
HLI	rs397507703
Exac	rs397507703
Gnomad	rs397507703
Varsome	rs397507703
LitVar	rs397507703
Map	rs397507703
PheGenI	rs397507703
Biobank	rs397507703
1000 genomes	rs397507703
hgdp	rs397507703
ensembl	rs397507703
geneview	rs397507703
scholar	rs397507703
google	rs397507703
pharmgkb	rs397507703
gwascentral	rs397507703
openSNP	rs397507703
23andMe	rs397507703
SNPshot	rs397507703
SNPdbe	rs397507703
MSV3d	rs397507703
GWAS Ctlg	rs397507703

Max Magnitude

6

ClinVar
Risk	rs397507703(-;-)
Alt	rs397507703(-;-)
Reference	Rs397507703(T;T)
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.32912587delT
CLNSRC	ClinVar
CLNACC	RCV000044348.2, RCV000257085.2,