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rs863225309

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225309(C;T)
Make rs863225309(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112819329
GeneAPC
is asnp
is mentioned by
dbSNPrs863225309
ebirs863225309
HLIrs863225309
Exacrs863225309
Varsomers863225309
Maprs863225309
PheGenIrs863225309
hapmaprs863225309
1000 genomesrs863225309
hgdprs863225309
ensemblrs863225309
gopubmedrs863225309
geneviewrs863225309
scholarrs863225309
googlers863225309
pharmgkbrs863225309
gwascentralrs863225309
openSNPrs863225309
23andMers863225309
23andMe allrs863225309
SNP Nexus

SNPshotrs863225309
SNPdbers863225309
MSV3drs863225309
GWAS Ctlgrs863225309
Max Magnitude0
ClinVar
Risk rs863225309(T;T)
Alt rs863225309(T;T)
Reference rs863225309(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112155026C>T
CLNSRC
CLNACC RCV000202128.1,