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rs863224458

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224458(G;T)
Make rs863224458(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112775629
GeneAPC
is asnp
is mentioned by
dbSNPrs863224458
ebirs863224458
HLIrs863224458
Exacrs863224458
Varsomers863224458
Maprs863224458
PheGenIrs863224458
hapmaprs863224458
1000 genomesrs863224458
hgdprs863224458
ensemblrs863224458
gopubmedrs863224458
geneviewrs863224458
scholarrs863224458
googlers863224458
pharmgkbrs863224458
gwascentralrs863224458
openSNPrs863224458
23andMers863224458
23andMe allrs863224458
SNP Nexus

SNPshotrs863224458
SNPdbers863224458
MSV3drs863224458
GWAS Ctlgrs863224458
Max Magnitude0
ClinVar
Risk rs863224458(T;T)
Alt rs863224458(T;T)
Reference rs863224458(G;G)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112111326G>T
CLNSRC
CLNACC RCV000199388.1,