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rs121917731

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121917731(C;T)
Make rs121917731(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position113043623
GeneMCC
is asnp
is mentioned by
dbSNPrs121917731
ebirs121917731
HLIrs121917731
Exacrs121917731
Varsomers121917731
Maprs121917731
PheGenIrs121917731
hapmaprs121917731
1000 genomesrs121917731
hgdprs121917731
ensemblrs121917731
gopubmedrs121917731
geneviewrs121917731
scholarrs121917731
googlers121917731
pharmgkbrs121917731
gwascentralrs121917731
openSNPrs121917731
23andMers121917731
23andMe allrs121917731
SNP Nexus

SNPshotrs121917731
SNPdbers121917731
MSV3drs121917731
GWAS Ctlgrs121917731
Max Magnitude0
OMIM159350
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121917731(T;T)
Alt rs121917731(T;T)
Reference rs121917731(C;C)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene MCC
CLNDBN Carcinoma of colon
Reversed 1
HGVS NC_000005.9:g.112379320G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000015266.4,