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rs587782774

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782774(A;G)
Make rs587782774(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32370400
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782774
ebirs587782774
HLIrs587782774
Exacrs587782774
Varsomers587782774
Maprs587782774
PheGenIrs587782774
hapmaprs587782774
1000 genomesrs587782774
hgdprs587782774
ensemblrs587782774
gopubmedrs587782774
geneviewrs587782774
scholarrs587782774
googlers587782774
pharmgkbrs587782774
gwascentralrs587782774
openSNPrs587782774
23andMers587782774
23andMe allrs587782774
SNP Nexus

SNPshotrs587782774
SNPdbers587782774
MSV3drs587782774
GWAS Ctlgrs587782774
Max Magnitude0
ClinVar
Risk rs587782774(G;G)
Alt rs587782774(G;G)
Reference rs587782774(A;A)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32944537A>G
CLNSRC
CLNACC RCV000132304.2,