rs483353118

Orientation

plus

Stabilized

plus

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

Make rs483353118(G;G)

Reference

GRCh38 38.1/142

Chromosome

13

Position

32355088

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs483353118
dbSNP (classic)	rs483353118
ClinGen	rs483353118
ebi	rs483353118
HLI	rs483353118
Exac	rs483353118
Gnomad	rs483353118
Varsome	rs483353118
LitVar	rs483353118
Map	rs483353118
PheGenI	rs483353118
Biobank	rs483353118
1000 genomes	rs483353118
hgdp	rs483353118
ensembl	rs483353118
geneview	rs483353118
scholar	rs483353118
google	rs483353118
pharmgkb	rs483353118
gwascentral	rs483353118
openSNP	rs483353118
23andMe	rs483353118
SNPshot	rs483353118
SNPdbe	rs483353118
MSV3d	rs483353118
GWAS Ctlg	rs483353118

Max Magnitude

6

ClinVar
Risk	rs483353118(G;G)
Alt	rs483353118(G;G)
Reference	Rs483353118(-;-)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32929225_32929226insG
CLNSRC	Breast Cancer Information Core (BRCA2)
CLNACC	RCV000113735.2,