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rs121913329

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913329(C;T)
Make rs121913329(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position112839726
GeneAPC
is asnp
is mentioned by
dbSNPrs121913329
dbSNP (classic)rs121913329
ClinGenrs121913329
ebirs121913329
HLIrs121913329
Exacrs121913329
Gnomadrs121913329
Varsomers121913329
LitVarrs121913329
Maprs121913329
PheGenIrs121913329
Biobankrs121913329
1000 genomesrs121913329
hgdprs121913329
ensemblrs121913329
geneviewrs121913329
scholarrs121913329
googlers121913329
pharmgkbrs121913329
gwascentralrs121913329
openSNPrs121913329
23andMers121913329
23andMe allrs121913329
SNPshotrs121913329
SNPdbers121913329
MSV3drs121913329
GWAS Ctlgrs121913329
Max Magnitude0
ClinVar
Risk rs121913329(T;T)
Alt rs121913329(T;T)
Reference Rs121913329(C;C)
Significance Probable-Pathogenic
Disease Colorectal Neoplasms
Variation info
Gene APC
CLNDBN Colorectal Neoplasms
Reversed 0
HGVS NC_000005.9:g.112175423C>T
CLNSRC
CLNACC RCV000443420.1,