rs397507709

Merged into

rs276174842

Orientation

plus

Stabilized

plus

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

Make rs397507709(TT;TT)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32338495

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507709
dbSNP (classic)	rs397507709
ClinGen	rs397507709
ebi	rs397507709
HLI	rs397507709
Exac	rs397507709
Gnomad	rs397507709
Varsome	rs397507709
LitVar	rs397507709
Map	rs397507709
PheGenI	rs397507709
Biobank	rs397507709
1000 genomes	rs397507709
hgdp	rs397507709
ensembl	rs397507709
geneview	rs397507709
scholar	rs397507709
google	rs397507709
pharmgkb	rs397507709
gwascentral	rs397507709
openSNP	rs397507709
23andMe	rs397507709
SNPshot	rs397507709
SNPdbe	rs397507709
MSV3d	rs397507709
GWAS Ctlg	rs397507709

Status

Merged into rs276174842

Max Magnitude

6

This SNP is functionally equivalent to rs276174842

ClinVar
Risk	rs397507709(TT;TT)
Alt	rs397507709(TT;TT)
Reference	Rs397507709(;)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer Hereditary cancer-predisposing syndrome
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 2 Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000013.10:g.32912631_32912632dupTT
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000044359.2, RCV000113279.2, RCV000130775.2,