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

rs121917732

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121917732(A;A)
Make rs121917732(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position113064110
GeneMCC
is asnp
is mentioned by
dbSNPrs121917732
ebirs121917732
HLIrs121917732
Exacrs121917732
Varsomers121917732
Maprs121917732
PheGenIrs121917732
hapmaprs121917732
1000 genomesrs121917732
hgdprs121917732
ensemblrs121917732
gopubmedrs121917732
geneviewrs121917732
scholarrs121917732
googlers121917732
pharmgkbrs121917732
gwascentralrs121917732
openSNPrs121917732
23andMers121917732
23andMe allrs121917732
SNP Nexus

SNPshotrs121917732
SNPdbers121917732
MSV3drs121917732
GWAS Ctlgrs121917732
Max Magnitude0
OMIM159350
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121917732(A;A)
Alt rs121917732(A;A)
Reference rs121917732(G;G)
Significance Pathogenic
Disease Carcinoma of colon
Variation info
Gene MCC
CLNDBN Carcinoma of colon
Reversed 1
HGVS NC_000005.9:g.112399807C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015267.4,