rs397507430

Orientation

plus

Stabilized

plus

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

Make rs397507430(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32396919

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507430
dbSNP (classic)	rs397507430
ClinGen	rs397507430
ebi	rs397507430
HLI	rs397507430
Exac	rs397507430
Gnomad	rs397507430
Varsome	rs397507430
LitVar	rs397507430
Map	rs397507430
PheGenI	rs397507430
Biobank	rs397507430
1000 genomes	rs397507430
hgdp	rs397507430
ensembl	rs397507430
geneview	rs397507430
scholar	rs397507430
google	rs397507430
pharmgkb	rs397507430
gwascentral	rs397507430
openSNP	rs397507430
23andMe	rs397507430
SNPshot	rs397507430
SNPdbe	rs397507430
MSV3d	rs397507430
GWAS Ctlg	rs397507430

Max Magnitude

6

ClinVar
Risk	rs397507430(T;T)
Alt	rs397507430(T;T)
Reference	Rs397507430(G;G)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32971056G>T
CLNSRC	ClinVar
CLNACC	RCV000031829.4,