rs397507760

Orientation

plus

Stabilized

plus

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

Make rs397507760(-;-)

Make rs397507760(-;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339486

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507760
dbSNP (classic)	rs397507760
ClinGen	rs397507760
ebi	rs397507760
HLI	rs397507760
Exac	rs397507760
Gnomad	rs397507760
Varsome	rs397507760
LitVar	rs397507760
Map	rs397507760
PheGenI	rs397507760
Biobank	rs397507760
1000 genomes	rs397507760
hgdp	rs397507760
ensembl	rs397507760
geneview	rs397507760
scholar	rs397507760
google	rs397507760
pharmgkb	rs397507760
gwascentral	rs397507760
openSNP	rs397507760
23andMe	rs397507760
SNPshot	rs397507760
SNPdbe	rs397507760
MSV3d	rs397507760
GWAS Ctlg	rs397507760

Max Magnitude

0

ClinVar
Risk	rs397507760(-;-)
Alt	rs397507760(-;-)
Reference	Rs397507760(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.32913623delG
CLNSRC	ClinVar
CLNACC	RCV000044565.2,