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rs587781471

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 6 BRCA2 variant considered pathogenic for breast cancer
Make rs587781471(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32336694
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587781471
dbSNP (old)rs587781471
ClinGenrs587781471
ebirs587781471
HLIrs587781471
Exacrs587781471
Varsomers587781471
Maprs587781471
PheGenIrs587781471
Biobankrs587781471
1000 genomesrs587781471
hgdprs587781471
ensemblrs587781471
gopubmedrs587781471
geneviewrs587781471
scholarrs587781471
googlers587781471
pharmgkbrs587781471
gwascentralrs587781471
openSNPrs587781471
23andMers587781471
23andMe allrs587781471
SNP Nexus

SNPshotrs587781471
SNPdbers587781471
MSV3drs587781471
GWAS Ctlgrs587781471
Max Magnitude6
ClinVar
Risk rs587781471(G;G)
Alt rs587781471(G;G)
Reference Rs587781471(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not specified Breast-ovarian cancer not provided
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome not specified Breast-ovarian cancer, familial 2 not provided
Reversed 0
HGVS NC_000013.10:g.32910831C>G
CLNSRC
CLNACC RCV000129415.3, RCV000238974.1, RCV000241405.2, RCV000484555.1,