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rs863225362

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225362(C;T)
Make rs863225362(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112775693
GeneAPC
is asnp
is mentioned by
dbSNPrs863225362
ebirs863225362
HLIrs863225362
Exacrs863225362
Varsomers863225362
Maprs863225362
PheGenIrs863225362
hapmaprs863225362
1000 genomesrs863225362
hgdprs863225362
ensemblrs863225362
gopubmedrs863225362
geneviewrs863225362
scholarrs863225362
googlers863225362
pharmgkbrs863225362
gwascentralrs863225362
openSNPrs863225362
23andMers863225362
23andMe allrs863225362
SNP Nexus

SNPshotrs863225362
SNPdbers863225362
MSV3drs863225362
GWAS Ctlgrs863225362
Max Magnitude0
ClinVar
Risk rs863225362(T;T)
Alt rs863225362(T;T)
Reference rs863225362(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112111390C>T
CLNSRC
CLNACC RCV000202083.1,