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rs863224281

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224281(C;T)
Make rs863224281(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112775683
GeneAPC
is asnp
is mentioned by
dbSNPrs863224281
ebirs863224281
HLIrs863224281
Exacrs863224281
Varsomers863224281
Maprs863224281
PheGenIrs863224281
hapmaprs863224281
1000 genomesrs863224281
hgdprs863224281
ensemblrs863224281
gopubmedrs863224281
geneviewrs863224281
scholarrs863224281
googlers863224281
pharmgkbrs863224281
gwascentralrs863224281
openSNPrs863224281
23andMers863224281
23andMe allrs863224281
SNP Nexus

SNPshotrs863224281
SNPdbers863224281
MSV3drs863224281
GWAS Ctlgrs863224281
Max Magnitude0
ClinVar
Risk rs863224281(G,T;G,T)
Alt rs863224281(G,T;G,T)
Reference rs863224281(C;C)
Significance Pathogenic
Disease not provided Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN not provided Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112111380C>G; NC_000005.9:g.112111380C>T
CLNSRC
CLNACC RCV000236674.1, RCV000198065.1,