rs397507858

Orientation

plus

Stabilized

plus

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

Make rs397507858(TA;TA)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340803

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507858
dbSNP (classic)	rs397507858
ClinGen	rs397507858
ebi	rs397507858
HLI	rs397507858
Exac	rs397507858
Gnomad	rs397507858
Varsome	rs397507858
LitVar	rs397507858
Map	rs397507858
PheGenI	rs397507858
Biobank	rs397507858
1000 genomes	rs397507858
hgdp	rs397507858
ensembl	rs397507858
geneview	rs397507858
scholar	rs397507858
google	rs397507858
pharmgkb	rs397507858
gwascentral	rs397507858
openSNP	rs397507858
23andMe	rs397507858
SNPshot	rs397507858
SNPdbe	rs397507858
MSV3d	rs397507858
GWAS Ctlg	rs397507858

Max Magnitude

6

ClinVar
Risk	rs397507858(TA;TA)
Alt	rs397507858(TA;TA)
Reference	Rs397507858(-;-)
Significance	Pathogenic
Disease	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer not provided
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast Hereditary cancer-predisposing syndrome Breast-ovarian cancer, familial 2 not provided
Reversed	0
HGVS	NC_000013.10:g.32914939_32914940dupTA
CLNSRC	ClinVar
CLNACC	RCV000044957.2, RCV000165176.1, RCV000238618.3, RCV000478202.1,