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rs121913462

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913462(G;T)
Make rs121913462(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112839510
GeneAPC
is asnp
is mentioned by
dbSNPrs121913462
dbSNP (old)rs121913462
ClinGenrs121913462
ebirs121913462
HLIrs121913462
Exacrs121913462
Gnomadrs121913462
Varsomers121913462
Maprs121913462
PheGenIrs121913462
Biobankrs121913462
1000 genomesrs121913462
hgdprs121913462
ensemblrs121913462
gopubmedrs121913462
geneviewrs121913462
scholarrs121913462
googlers121913462
pharmgkbrs121913462
gwascentralrs121913462
openSNPrs121913462
23andMers121913462
23andMe allrs121913462
SNPshotrs121913462
SNPdbers121913462
MSV3drs121913462
GWAS Ctlgrs121913462
Max Magnitude0
ClinVar
Risk rs121913462(A;A) rs121913462(T;T)
Alt rs121913462(A;A) rs121913462(T;T)
Reference Rs121913462(G;G)
Significance Probable-Pathogenic
Disease Colorectal Neoplasms
Variation info
Gene APC
CLNDBN Colorectal Neoplasms
Reversed 0
HGVS NC_000005.9:g.112175207G>T
CLNSRC
CLNACC RCV000443324.1,