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rs121913326

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913326(G;T)
Make rs121913326(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112839729
GeneAPC
is asnp
is mentioned by
dbSNPrs121913326
dbSNP (old)rs121913326
ClinGenrs121913326
ebirs121913326
HLIrs121913326
Exacrs121913326
Gnomadrs121913326
Varsomers121913326
Maprs121913326
PheGenIrs121913326
Biobankrs121913326
1000 genomesrs121913326
hgdprs121913326
ensemblrs121913326
gopubmedrs121913326
geneviewrs121913326
scholarrs121913326
googlers121913326
pharmgkbrs121913326
gwascentralrs121913326
openSNPrs121913326
23andMers121913326
23andMe allrs121913326
SNPshotrs121913326
SNPdbers121913326
MSV3drs121913326
GWAS Ctlgrs121913326
Max Magnitude0
ClinVar
Risk rs121913326(T;T)
Alt rs121913326(T;T)
Reference Rs121913326(G;G)
Significance Probable-Pathogenic
Disease Colorectal Neoplasms
Variation info
Gene APC
CLNDBN Colorectal Neoplasms
Reversed 0
HGVS NC_000005.9:g.112175426G>T
CLNSRC
CLNACC RCV000426216.1,