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rs587779212

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779212(C;T)
Make rs587779212(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799466
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779212
ebirs587779212
HLIrs587779212
Exacrs587779212
Varsomers587779212
Maprs587779212
PheGenIrs587779212
hapmaprs587779212
1000 genomesrs587779212
hgdprs587779212
ensemblrs587779212
gopubmedrs587779212
geneviewrs587779212
scholarrs587779212
googlers587779212
pharmgkbrs587779212
gwascentralrs587779212
openSNPrs587779212
23andMers587779212
23andMe allrs587779212
SNP Nexus

SNPshotrs587779212
SNPdbers587779212
MSV3drs587779212
GWAS Ctlgrs587779212
Max Magnitude0
ClinVar
Risk rs587779212(T;T)
Alt rs587779212(T;T)
Reference rs587779212(C;C)
Significance Other
Disease Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation info
Gene MSH6
CLNDBN Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000002.11:g.48026605C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074659.2, RCV000131420.2, RCV000202276.2,