rs56383036

Orientation

plus

Stabilized

plus

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

Make rs56383036(C;C)

Make rs56383036(C;G)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

32330949

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs56383036
dbSNP (classic)	rs56383036
ClinGen	rs56383036
ebi	rs56383036
HLI	rs56383036
Exac	rs56383036
Gnomad	rs56383036
Varsome	rs56383036
LitVar	rs56383036
Map	rs56383036
PheGenI	rs56383036
Biobank	rs56383036
1000 genomes	rs56383036
hgdp	rs56383036
ensembl	rs56383036
geneview	rs56383036
scholar	rs56383036
google	rs56383036
pharmgkb	rs56383036
gwascentral	rs56383036
openSNP	rs56383036
23andMe	rs56383036
SNPshot	rs56383036
SNPdbe	rs56383036
MSV3d	rs56383036
GWAS Ctlg	rs56383036

Max Magnitude

6

ClinVar
Risk	rs56383036(C;C) rs56383036(T;T)
Alt	rs56383036(C;C) rs56383036(T;T)
Reference	Rs56383036(G;G)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32905086G>T
CLNSRC
CLNACC	RCV000162051.3,