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rs587779215

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779215(C;G)
Make rs587779215(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47799555
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779215
ebirs587779215
HLIrs587779215
Exacrs587779215
Varsomers587779215
Maprs587779215
PheGenIrs587779215
hapmaprs587779215
1000 genomesrs587779215
hgdprs587779215
ensemblrs587779215
gopubmedrs587779215
geneviewrs587779215
scholarrs587779215
googlers587779215
pharmgkbrs587779215
gwascentralrs587779215
openSNPrs587779215
23andMers587779215
23andMe allrs587779215
SNP Nexus

SNPshotrs587779215
SNPdbers587779215
MSV3drs587779215
GWAS Ctlgrs587779215
Max Magnitude0
ClinVar
Risk rs587779215(G;G)
Alt rs587779215(G;G)
Reference rs587779215(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48026694C>G
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074665.2,