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rs121913331

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913331(C;T)
Make rs121913331(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112838934
GeneAPC
is asnp
is mentioned by
dbSNPrs121913331
ebirs121913331
HLIrs121913331
Exacrs121913331
Varsomers121913331
Maprs121913331
PheGenIrs121913331
hapmaprs121913331
1000 genomesrs121913331
hgdprs121913331
ensemblrs121913331
gopubmedrs121913331
geneviewrs121913331
scholarrs121913331
googlers121913331
pharmgkbrs121913331
gwascentralrs121913331
openSNPrs121913331
23andMers121913331
23andMe allrs121913331
SNP Nexus

SNPshotrs121913331
SNPdbers121913331
MSV3drs121913331
GWAS Ctlgrs121913331
Max Magnitude0
ClinVar
Risk rs121913331(A,T;A,T)
Alt rs121913331(A,T;A,T)
Reference rs121913331(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112174631C>T
CLNSRC
CLNACC RCV000228687.1,