rs397508036

Orientation

plus

Stabilized

plus

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

Make rs397508036(C;C)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32379896

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs397508036
dbSNP (classic)	rs397508036
ClinGen	rs397508036
ebi	rs397508036
HLI	rs397508036
Exac	rs397508036
Gnomad	rs397508036
Varsome	rs397508036
LitVar	rs397508036
Map	rs397508036
PheGenI	rs397508036
Biobank	rs397508036
1000 genomes	rs397508036
hgdp	rs397508036
ensembl	rs397508036
geneview	rs397508036
scholar	rs397508036
google	rs397508036
pharmgkb	rs397508036
gwascentral	rs397508036
openSNP	rs397508036
23andMe	rs397508036
SNPshot	rs397508036
SNPdbe	rs397508036
MSV3d	rs397508036
GWAS Ctlg	rs397508036

Max Magnitude

6

aka c.9100dupC

ClinVar
Risk	rs397508036(C;C)
Alt	rs397508036(C;C)
Reference	Rs397508036(-;-)
Significance	Untested
Disease	Familial cancer of breast
Variation	info
Gene	BRCA2
CLNDBN	Familial cancer of breast
Reversed	0
HGVS	NC_000013.10:g.32954033dupC
CLNSRC	ClinVar
CLNACC	RCV000045715.2,