Have questions? Visit https://www.reddit.com/r/SNPedia

rs587779227

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587779227(A;A)
Make rs587779227(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800040
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779227
ebirs587779227
HLIrs587779227
Exacrs587779227
Varsomers587779227
Maprs587779227
PheGenIrs587779227
hapmaprs587779227
1000 genomesrs587779227
hgdprs587779227
ensemblrs587779227
gopubmedrs587779227
geneviewrs587779227
scholarrs587779227
googlers587779227
pharmgkbrs587779227
gwascentralrs587779227
openSNPrs587779227
23andMers587779227
23andMe allrs587779227
SNP Nexus

SNPshotrs587779227
SNPdbers587779227
MSV3drs587779227
GWAS Ctlgrs587779227
Max Magnitude0
ClinVar
Risk rs587779227(A;A)
Alt rs587779227(A;A)
Reference rs587779227(G;G)
Significance Probable-Pathogenic
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.48027179G>A
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074709.3, RCV000128865.4, RCV000212657.1,