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rs863225316

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225316(A;A)
Make rs863225316(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112827928
GeneAPC
is asnp
is mentioned by
dbSNPrs863225316
ebirs863225316
HLIrs863225316
Exacrs863225316
Varsomers863225316
Maprs863225316
PheGenIrs863225316
hapmaprs863225316
1000 genomesrs863225316
hgdprs863225316
ensemblrs863225316
gopubmedrs863225316
geneviewrs863225316
scholarrs863225316
googlers863225316
pharmgkbrs863225316
gwascentralrs863225316
openSNPrs863225316
23andMers863225316
23andMe allrs863225316
SNP Nexus

SNPshotrs863225316
SNPdbers863225316
MSV3drs863225316
GWAS Ctlgrs863225316
Max Magnitude0
ClinVar
Risk rs863225316(A;A)
Alt rs863225316(A;A)
Reference rs863225316(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112163625G>A
CLNSRC
CLNACC RCV000202184.1,