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rs863225314

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863225314(G;G)
Make rs863225314(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112827132
GeneAPC
is asnp
is mentioned by
dbSNPrs863225314
ebirs863225314
HLIrs863225314
Exacrs863225314
Varsomers863225314
Maprs863225314
PheGenIrs863225314
hapmaprs863225314
1000 genomesrs863225314
hgdprs863225314
ensemblrs863225314
gopubmedrs863225314
geneviewrs863225314
scholarrs863225314
googlers863225314
pharmgkbrs863225314
gwascentralrs863225314
openSNPrs863225314
23andMers863225314
23andMe allrs863225314
SNP Nexus

SNPshotrs863225314
SNPdbers863225314
MSV3drs863225314
GWAS Ctlgrs863225314
Max Magnitude0
ClinVar
Risk rs863225314(G;G)
Alt rs863225314(G;G)
Reference rs863225314(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112162829T>G
CLNSRC
CLNACC RCV000202053.1,