rs397507945

Orientation

plus

Stabilized

plus

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

Make rs397507945(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32362680

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507945
dbSNP (classic)	rs397507945
ClinGen	rs397507945
ebi	rs397507945
HLI	rs397507945
Exac	rs397507945
Gnomad	rs397507945
Varsome	rs397507945
LitVar	rs397507945
Map	rs397507945
PheGenI	rs397507945
Biobank	rs397507945
1000 genomes	rs397507945
hgdp	rs397507945
ensembl	rs397507945
geneview	rs397507945
scholar	rs397507945
google	rs397507945
pharmgkb	rs397507945
gwascentral	rs397507945
openSNP	rs397507945
23andMe	rs397507945
SNPshot	rs397507945
SNPdbe	rs397507945
MSV3d	rs397507945
GWAS Ctlg	rs397507945

Max Magnitude

6

aka c.7963delC

ClinVar
Risk	rs397507945(-;-)
Alt	rs397507945(-;-)
Reference	Rs397507945(C;C)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32936817delC
CLNSRC	ClinVar
CLNACC	RCV000045358.2,