rs397507980

Orientation

plus

Stabilized

plus

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

Make rs397507980(C;C)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32370418

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397507980
dbSNP (classic)	rs397507980
ClinGen	rs397507980
ebi	rs397507980
HLI	rs397507980
Exac	rs397507980
Gnomad	rs397507980
Varsome	rs397507980
LitVar	rs397507980
Map	rs397507980
PheGenI	rs397507980
Biobank	rs397507980
1000 genomes	rs397507980
hgdp	rs397507980
ensembl	rs397507980
geneview	rs397507980
scholar	rs397507980
google	rs397507980
pharmgkb	rs397507980
gwascentral	rs397507980
openSNP	rs397507980
23andMe	rs397507980
SNPshot	rs397507980
SNPdbe	rs397507980
MSV3d	rs397507980
GWAS Ctlg	rs397507980

Max Magnitude

6

aka c.8348dupC

ClinVar
Risk	rs397507980(C;C)
Alt	rs397507980(C;C)
Reference	Rs397507980(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32944555dupC
CLNSRC	ClinVar
CLNACC	RCV000045486.2,