rs397508034

Orientation

plus

Stabilized

plus

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

Make rs397508034(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379870

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508034
dbSNP (classic)	rs397508034
ClinGen	rs397508034
ebi	rs397508034
HLI	rs397508034
Exac	rs397508034
Gnomad	rs397508034
Varsome	rs397508034
LitVar	rs397508034
Map	rs397508034
PheGenI	rs397508034
Biobank	rs397508034
1000 genomes	rs397508034
hgdp	rs397508034
ensembl	rs397508034
geneview	rs397508034
scholar	rs397508034
google	rs397508034
pharmgkb	rs397508034
gwascentral	rs397508034
openSNP	rs397508034
23andMe	rs397508034
SNPshot	rs397508034
SNPdbe	rs397508034
MSV3d	rs397508034
GWAS Ctlg	rs397508034

Max Magnitude

6

ClinVar
Risk	rs397508034(-;-)
Alt	rs397508034(-;-)
Reference	Rs397508034(AT;AT)
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.32954007_32954008delTA
CLNSRC	ClinVar
CLNACC	RCV000045704.2, RCV000257553.2,