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rs587781659

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781659(-;-)
Make rs587781659(-;C)
Make rs587781659(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800947
GeneMSH6
is asnp
is mentioned by
dbSNPrs587781659
ebirs587781659
HLIrs587781659
Exacrs587781659
Varsomers587781659
Maprs587781659
PheGenIrs587781659
hapmaprs587781659
1000 genomesrs587781659
hgdprs587781659
ensemblrs587781659
gopubmedrs587781659
geneviewrs587781659
scholarrs587781659
googlers587781659
pharmgkbrs587781659
gwascentralrs587781659
openSNPrs587781659
23andMers587781659
23andMe allrs587781659
SNP Nexus

SNPshotrs587781659
SNPdbers587781659
MSV3drs587781659
GWAS Ctlgrs587781659
Max Magnitude0
ClinVar
Risk rs587781659(C;C)
Alt rs587781659(C;C)
Reference rs587781659(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48028086dupC
CLNSRC
CLNACC RCV000129802.2,