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rs863225351

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225351(-;T)
Make rs863225351(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112839619
GeneAPC
is asnp
is mentioned by
dbSNPrs863225351
ClinGenrs863225351
ebirs863225351
HLIrs863225351
Exacrs863225351
Varsomers863225351
Maprs863225351
PheGenIrs863225351
hapmaprs863225351
1000 genomesrs863225351
hgdprs863225351
ensemblrs863225351
gopubmedrs863225351
geneviewrs863225351
scholarrs863225351
googlers863225351
pharmgkbrs863225351
gwascentralrs863225351
openSNPrs863225351
23andMers863225351
23andMe allrs863225351
SNP Nexus

SNPshotrs863225351
SNPdbers863225351
MSV3drs863225351
GWAS Ctlgrs863225351
Max Magnitude0
ClinVar
Risk rs863225351(T;T)
Alt rs863225351(T;T)
Reference Rs863225351(;)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112175316dupT
CLNSRC
CLNACC RCV000202185.1,