rs397507424

Orientation

plus

Stabilized

plus

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

Make rs397507424(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32394706

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507424
dbSNP (classic)	rs397507424
ClinGen	rs397507424
ebi	rs397507424
HLI	rs397507424
Exac	rs397507424
Gnomad	rs397507424
Varsome	rs397507424
LitVar	rs397507424
Map	rs397507424
PheGenI	rs397507424
Biobank	rs397507424
1000 genomes	rs397507424
hgdp	rs397507424
ensembl	rs397507424
geneview	rs397507424
scholar	rs397507424
google	rs397507424
pharmgkb	rs397507424
gwascentral	rs397507424
openSNP	rs397507424
23andMe	rs397507424
SNPshot	rs397507424
SNPdbe	rs397507424
MSV3d	rs397507424
GWAS Ctlg	rs397507424

Max Magnitude

6

ClinVar
Risk	rs397507424(-;-)
Alt	rs397507424(-;-)
Reference	Rs397507424(T;T)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32968843delT
CLNSRC	ClinVar
CLNACC	RCV000031809.4,