rs397507581

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs397507581(G;T)

Make rs397507581(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32319142

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507581
dbSNP (classic)	rs397507581
ClinGen	rs397507581
ebi	rs397507581
HLI	rs397507581
Exac	rs397507581
Gnomad	rs397507581
Varsome	rs397507581
LitVar	rs397507581
Map	rs397507581
PheGenI	rs397507581
Biobank	rs397507581
1000 genomes	rs397507581
hgdp	rs397507581
ensembl	rs397507581
geneview	rs397507581
scholar	rs397507581
google	rs397507581
pharmgkb	rs397507581
gwascentral	rs397507581
openSNP	rs397507581
23andMe	rs397507581
SNPshot	rs397507581
SNPdbe	rs397507581
MSV3d	rs397507581
GWAS Ctlg	rs397507581

Max Magnitude

0

ClinVar
Risk	rs397507581(T;T)
Alt	rs397507581(T;T)
Reference	Rs397507581(G;G)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32893279G>T
CLNSRC	ClinVar
CLNACC	RCV000043784.2,