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rs121913332

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121913332(C;T)
Make rs121913332(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112839942
GeneAPC
is asnp
is mentioned by
dbSNPrs121913332
ebirs121913332
HLIrs121913332
Exacrs121913332
Varsomers121913332
Maprs121913332
PheGenIrs121913332
hapmaprs121913332
1000 genomesrs121913332
hgdprs121913332
ensemblrs121913332
gopubmedrs121913332
geneviewrs121913332
scholarrs121913332
googlers121913332
pharmgkbrs121913332
gwascentralrs121913332
openSNPrs121913332
23andMers121913332
23andMe allrs121913332
SNP Nexus

SNPshotrs121913332
SNPdbers121913332
MSV3drs121913332
GWAS Ctlgrs121913332
Max Magnitude0
ClinVar
Risk rs121913332(G,T;G,T)
Alt rs121913332(G,T;G,T)
Reference rs121913332(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.112175639C>T
CLNSRC
CLNACC RCV000174977.3,