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rs863224455

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224455(C;T)
Make rs863224455(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112819104
GeneAPC
is asnp
is mentioned by
dbSNPrs863224455
ebirs863224455
HLIrs863224455
Exacrs863224455
Varsomers863224455
Maprs863224455
PheGenIrs863224455
hapmaprs863224455
1000 genomesrs863224455
hgdprs863224455
ensemblrs863224455
gopubmedrs863224455
geneviewrs863224455
scholarrs863224455
googlers863224455
pharmgkbrs863224455
gwascentralrs863224455
openSNPrs863224455
23andMers863224455
23andMe allrs863224455
SNP Nexus

SNPshotrs863224455
SNPdbers863224455
MSV3drs863224455
GWAS Ctlgrs863224455
Max Magnitude0
ClinVar
Risk rs863224455(T;T)
Alt rs863224455(T;T)
Reference rs863224455(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.112154801C>T
CLNSRC
CLNACC RCV000198412.1,