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rs587779231

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587779231(C;C)
Make rs587779231(C;T)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position47800100
GeneMSH6
is asnp
is mentioned by
dbSNPrs587779231
ebirs587779231
HLIrs587779231
Exacrs587779231
Varsomers587779231
Maprs587779231
PheGenIrs587779231
hapmaprs587779231
1000 genomesrs587779231
hgdprs587779231
ensemblrs587779231
gopubmedrs587779231
geneviewrs587779231
scholarrs587779231
googlers587779231
pharmgkbrs587779231
gwascentralrs587779231
openSNPrs587779231
23andMers587779231
23andMe allrs587779231
SNP Nexus

SNPshotrs587779231
SNPdbers587779231
MSV3drs587779231
GWAS Ctlgrs587779231
Max Magnitude0
ClinVar
Risk rs587779231(C;C)
Alt rs587779231(C;C)
Reference rs587779231(T;T)
Significance Probable-Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48027239T>C
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000074718.2,