rs397507823

Orientation

plus

Stabilized

plus

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

Make rs397507823(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340388

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507823
dbSNP (classic)	rs397507823
ClinGen	rs397507823
ebi	rs397507823
HLI	rs397507823
Exac	rs397507823
Gnomad	rs397507823
Varsome	rs397507823
LitVar	rs397507823
Map	rs397507823
PheGenI	rs397507823
Biobank	rs397507823
1000 genomes	rs397507823
hgdp	rs397507823
ensembl	rs397507823
geneview	rs397507823
scholar	rs397507823
google	rs397507823
pharmgkb	rs397507823
gwascentral	rs397507823
openSNP	rs397507823
23andMe	rs397507823
SNPshot	rs397507823
SNPdbe	rs397507823
MSV3d	rs397507823
GWAS Ctlg	rs397507823

Merged from

Rs765284298

Max Magnitude

6

ClinVar
Risk	rs397507823(-;-)
Alt	rs397507823(-;-)
Reference	Rs397507823(TT;TT)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32914525_32914526delTT
CLNSRC	ClinVar
CLNACC	RCV000044824.2, RCV000165674.1, RCV000241414.2,