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rs863225313

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225313(G;T)
Make rs863225313(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112827107
GeneAPC
is asnp
is mentioned by
dbSNPrs863225313
ebirs863225313
HLIrs863225313
Exacrs863225313
Varsomers863225313
Maprs863225313
PheGenIrs863225313
hapmaprs863225313
1000 genomesrs863225313
hgdprs863225313
ensemblrs863225313
gopubmedrs863225313
geneviewrs863225313
scholarrs863225313
googlers863225313
pharmgkbrs863225313
gwascentralrs863225313
openSNPrs863225313
23andMers863225313
23andMe allrs863225313
SNP Nexus

SNPshotrs863225313
SNPdbers863225313
MSV3drs863225313
GWAS Ctlgrs863225313
Max Magnitude0
ClinVar
Risk rs863225313(T;T)
Alt rs863225313(T;T)
Reference rs863225313(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112162804G>T
CLNSRC
CLNACC RCV000202308.1,