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rs863225356

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225356(C;G)
Make rs863225356(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112840228
GeneAPC
is asnp
is mentioned by
dbSNPrs863225356
ebirs863225356
HLIrs863225356
Exacrs863225356
Varsomers863225356
Maprs863225356
PheGenIrs863225356
hapmaprs863225356
1000 genomesrs863225356
hgdprs863225356
ensemblrs863225356
gopubmedrs863225356
geneviewrs863225356
scholarrs863225356
googlers863225356
pharmgkbrs863225356
gwascentralrs863225356
openSNPrs863225356
23andMers863225356
23andMe allrs863225356
SNP Nexus

SNPshotrs863225356
SNPdbers863225356
MSV3drs863225356
GWAS Ctlgrs863225356
Max Magnitude0
ClinVar
Risk rs863225356(G;G)
Alt rs863225356(G;G)
Reference rs863225356(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112175925C>G
CLNSRC
CLNACC RCV000202021.1,