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

rs121913327

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913327(C;T)
Make rs121913327(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position112839606
GeneAPC
is asnp
is mentioned by
dbSNPrs121913327
ebirs121913327
HLIrs121913327
Exacrs121913327
Varsomers121913327
Maprs121913327
PheGenIrs121913327
hapmaprs121913327
1000 genomesrs121913327
hgdprs121913327
ensemblrs121913327
gopubmedrs121913327
geneviewrs121913327
scholarrs121913327
googlers121913327
pharmgkbrs121913327
gwascentralrs121913327
openSNPrs121913327
23andMers121913327
23andMe allrs121913327
SNP Nexus

SNPshotrs121913327
SNPdbers121913327
MSV3drs121913327
GWAS Ctlgrs121913327
Max Magnitude0
OMIM611731
Desc
Variant0009
Relatedalso
ClinVar
Risk rs121913327(T;T)
Alt rs121913327(T;T)
Reference rs121913327(C;C)
Significance Pathogenic
Disease Carcinoma of colon Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Carcinoma of colon Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112175303C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000838.6, RCV000168134.1,