rs397507756

Orientation

plus

Stabilized

plus

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

Make rs397507756(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32339400

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507756
dbSNP (classic)	rs397507756
ClinGen	rs397507756
ebi	rs397507756
HLI	rs397507756
Exac	rs397507756
Gnomad	rs397507756
Varsome	rs397507756
LitVar	rs397507756
Map	rs397507756
PheGenI	rs397507756
Biobank	rs397507756
1000 genomes	rs397507756
hgdp	rs397507756
ensembl	rs397507756
geneview	rs397507756
scholar	rs397507756
google	rs397507756
pharmgkb	rs397507756
gwascentral	rs397507756
openSNP	rs397507756
23andMe	rs397507756
SNPshot	rs397507756
SNPdbe	rs397507756
MSV3d	rs397507756
GWAS Ctlg	rs397507756

Max Magnitude

6

aka c.5045delG (p.Ser1682Ilefs)

23andMe name: i5009119

ClinVar
Risk	rs397507756(-;-)
Alt	rs397507756(-;-)
Reference	Rs397507756(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.32913537delG
CLNSRC	ClinVar
CLNACC	RCV000044544.2,