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rs863225321

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225321(A;A)
Make rs863225321(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112837552
GeneAPC
is asnp
is mentioned by
dbSNPrs863225321
ebirs863225321
HLIrs863225321
Exacrs863225321
Varsomers863225321
Maprs863225321
PheGenIrs863225321
hapmaprs863225321
1000 genomesrs863225321
hgdprs863225321
ensemblrs863225321
gopubmedrs863225321
geneviewrs863225321
scholarrs863225321
googlers863225321
pharmgkbrs863225321
gwascentralrs863225321
openSNPrs863225321
23andMers863225321
23andMe allrs863225321
SNP Nexus

SNPshotrs863225321
SNPdbers863225321
MSV3drs863225321
GWAS Ctlgrs863225321
Max Magnitude0
ClinVar
Risk rs863225321(A;A)
Alt rs863225321(A;A)
Reference rs863225321(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112173249G>A
CLNSRC
CLNACC RCV000202143.1,