rs397507806

Orientation

plus

Stabilized

plus

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

Make rs397507806(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340144

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507806
dbSNP (classic)	rs397507806
ClinGen	rs397507806
ebi	rs397507806
HLI	rs397507806
Exac	rs397507806
Gnomad	rs397507806
Varsome	rs397507806
LitVar	rs397507806
Map	rs397507806
PheGenI	rs397507806
Biobank	rs397507806
1000 genomes	rs397507806
hgdp	rs397507806
ensembl	rs397507806
geneview	rs397507806
scholar	rs397507806
google	rs397507806
pharmgkb	rs397507806
gwascentral	rs397507806
openSNP	rs397507806
23andMe	rs397507806
SNPshot	rs397507806
SNPdbe	rs397507806
MSV3d	rs397507806
GWAS Ctlg	rs397507806

Max Magnitude

6

ClinVar
Risk	rs397507806(-;-)
Alt	rs397507806(-;-)
Reference	Rs397507806(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.32914281delT
CLNSRC	ClinVar
CLNACC	RCV000044757.2, RCV000256614.2,