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rs863225307

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225307(C;T)
Make rs863225307(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112819077
GeneAPC
is asnp
is mentioned by
dbSNPrs863225307
ebirs863225307
HLIrs863225307
Exacrs863225307
Varsomers863225307
Maprs863225307
PheGenIrs863225307
hapmaprs863225307
1000 genomesrs863225307
hgdprs863225307
ensemblrs863225307
gopubmedrs863225307
geneviewrs863225307
scholarrs863225307
googlers863225307
pharmgkbrs863225307
gwascentralrs863225307
openSNPrs863225307
23andMers863225307
23andMe allrs863225307
SNP Nexus

SNPshotrs863225307
SNPdbers863225307
MSV3drs863225307
GWAS Ctlgrs863225307
Max Magnitude0
ClinVar
Risk rs863225307(T;T)
Alt rs863225307(T;T)
Reference rs863225307(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112154774C>T
CLNSRC
CLNACC RCV000202206.1,