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rs863225365

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225365(A;A)
Make rs863225365(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112775739
GeneAPC
is asnp
is mentioned by
dbSNPrs863225365
ebirs863225365
HLIrs863225365
Exacrs863225365
Varsomers863225365
Maprs863225365
PheGenIrs863225365
hapmaprs863225365
1000 genomesrs863225365
hgdprs863225365
ensemblrs863225365
gopubmedrs863225365
geneviewrs863225365
scholarrs863225365
googlers863225365
pharmgkbrs863225365
gwascentralrs863225365
openSNPrs863225365
23andMers863225365
23andMe allrs863225365
SNP Nexus

SNPshotrs863225365
SNPdbers863225365
MSV3drs863225365
GWAS Ctlgrs863225365
Max Magnitude0
ClinVar
Risk rs863225365(A,C;A,C)
Alt rs863225365(A,C;A,C)
Reference rs863225365(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112111436T>A; NC_000005.9:g.112111436T>C
CLNSRC
CLNACC RCV000202121.1, RCV000202262.1,