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rs863225348

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225348(C;G)
Make rs863225348(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112839409
GeneAPC
is asnp
is mentioned by
dbSNPrs863225348
ebirs863225348
HLIrs863225348
Exacrs863225348
Varsomers863225348
Maprs863225348
PheGenIrs863225348
hapmaprs863225348
1000 genomesrs863225348
hgdprs863225348
ensemblrs863225348
gopubmedrs863225348
geneviewrs863225348
scholarrs863225348
googlers863225348
pharmgkbrs863225348
gwascentralrs863225348
openSNPrs863225348
23andMers863225348
23andMe allrs863225348
SNP Nexus

SNPshotrs863225348
SNPdbers863225348
MSV3drs863225348
GWAS Ctlgrs863225348
Max Magnitude0
ClinVar
Risk rs863225348(G;G)
Alt rs863225348(G;G)
Reference rs863225348(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112175106C>G
CLNSRC
CLNACC RCV000202286.1,