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rs121913328

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913328(C;T)
Make rs121913328(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112839693
GeneAPC
is asnp
is mentioned by
dbSNPrs121913328
dbSNP (old)rs121913328
ClinGenrs121913328
ebirs121913328
HLIrs121913328
Exacrs121913328
Gnomadrs121913328
Varsomers121913328
Maprs121913328
PheGenIrs121913328
Biobankrs121913328
1000 genomesrs121913328
hgdprs121913328
ensemblrs121913328
gopubmedrs121913328
geneviewrs121913328
scholarrs121913328
googlers121913328
pharmgkbrs121913328
gwascentralrs121913328
openSNPrs121913328
23andMers121913328
23andMe allrs121913328
SNPshotrs121913328
SNPdbers121913328
MSV3drs121913328
GWAS Ctlgrs121913328
Max Magnitude0
ClinVar
Risk rs121913328(T;T)
Alt rs121913328(T;T)
Reference Rs121913328(C;C)
Significance Probable-Pathogenic
Disease Colorectal Neoplasms
Variation info
Gene APC
CLNDBN Colorectal Neoplasms
Reversed 0
HGVS NC_000005.9:g.112175390C>T
CLNSRC
CLNACC RCV000433625.1,