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rs587782161

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587782161(-;-)
Make rs587782161(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome13
Position32339938
GeneBRCA2
is asnp
is mentioned by
dbSNPrs587782161
ebirs587782161
HLIrs587782161
Exacrs587782161
Varsomers587782161
Maprs587782161
PheGenIrs587782161
hapmaprs587782161
1000 genomesrs587782161
hgdprs587782161
ensemblrs587782161
gopubmedrs587782161
geneviewrs587782161
scholarrs587782161
googlers587782161
pharmgkbrs587782161
gwascentralrs587782161
openSNPrs587782161
23andMers587782161
23andMe allrs587782161
SNP Nexus

SNPshotrs587782161
SNPdbers587782161
MSV3drs587782161
GWAS Ctlgrs587782161
Max Magnitude0
ClinVar
Risk rs587782161(;)
Alt rs587782161(;)
Reference rs587782161(A;A)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene BRCA2
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000013.10:g.32914075delA
CLNSRC
CLNACC RCV000130752.2,