rs397507898

Orientation

plus

Stabilized

plus

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

Make rs397507898(-;-)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32355019

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507898
dbSNP (classic)	rs397507898
ClinGen	rs397507898
ebi	rs397507898
HLI	rs397507898
Exac	rs397507898
Gnomad	rs397507898
Varsome	rs397507898
LitVar	rs397507898
Map	rs397507898
PheGenI	rs397507898
Biobank	rs397507898
1000 genomes	rs397507898
hgdp	rs397507898
ensembl	rs397507898
geneview	rs397507898
scholar	rs397507898
google	rs397507898
pharmgkb	rs397507898
gwascentral	rs397507898
openSNP	rs397507898
23andMe	rs397507898
SNPshot	rs397507898
SNPdbe	rs397507898
MSV3d	rs397507898
GWAS Ctlg	rs397507898

Max Magnitude

6

aka c.7166delG

ClinVar
Risk	rs397507898(-;-)
Alt	rs397507898(-;-)
Reference	Rs397507898(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.32929156delG
CLNSRC	ClinVar
CLNACC	RCV000045153.2,