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rs56383036

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs56383036(C;C)
Make rs56383036(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32330949
GeneBRCA2
is asnp
is mentioned by
dbSNPrs56383036
ebirs56383036
HLIrs56383036
Exacrs56383036
Varsomers56383036
Maprs56383036
PheGenIrs56383036
hapmaprs56383036
1000 genomesrs56383036
hgdprs56383036
ensemblrs56383036
gopubmedrs56383036
geneviewrs56383036
scholarrs56383036
googlers56383036
pharmgkbrs56383036
gwascentralrs56383036
openSNPrs56383036
23andMers56383036
23andMe allrs56383036
SNP Nexus

SNPshotrs56383036
SNPdbers56383036
MSV3drs56383036
GWAS Ctlgrs56383036
Max Magnitude0
ClinVar
Risk rs56383036(C,T;C,T)
Alt rs56383036(C,T;C,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 RCV000162051.1,