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rs587781691

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781691(-;-)
Make rs587781691(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47798725
GeneMSH6
is asnp
is mentioned by
dbSNPrs587781691
ebirs587781691
HLIrs587781691
Exacrs587781691
Varsomers587781691
Maprs587781691
PheGenIrs587781691
hapmaprs587781691
1000 genomesrs587781691
hgdprs587781691
ensemblrs587781691
gopubmedrs587781691
geneviewrs587781691
scholarrs587781691
googlers587781691
pharmgkbrs587781691
gwascentralrs587781691
openSNPrs587781691
23andMers587781691
23andMe allrs587781691
SNP Nexus

SNPshotrs587781691
SNPdbers587781691
MSV3drs587781691
GWAS Ctlgrs587781691
Max Magnitude0
ClinVar
Risk rs587781691(;)
Alt rs587781691(;)
Reference rs587781691(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene MSH6
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000002.11:g.48025864delC
CLNSRC
CLNACC RCV000129856.2,