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rs863225347

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225347(A;A)
Make rs863225347(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112839404
GeneAPC
is asnp
is mentioned by
dbSNPrs863225347
ebirs863225347
HLIrs863225347
Exacrs863225347
Varsomers863225347
Maprs863225347
PheGenIrs863225347
hapmaprs863225347
1000 genomesrs863225347
hgdprs863225347
ensemblrs863225347
gopubmedrs863225347
geneviewrs863225347
scholarrs863225347
googlers863225347
pharmgkbrs863225347
gwascentralrs863225347
openSNPrs863225347
23andMers863225347
23andMe allrs863225347
SNP Nexus

SNPshotrs863225347
SNPdbers863225347
MSV3drs863225347
GWAS Ctlgrs863225347
Max Magnitude0
ClinVar
Risk rs863225347(A;A)
Alt rs863225347(A;A)
Reference rs863225347(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112175101T>A
CLNSRC
CLNACC RCV000202149.2,