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rs863225326

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225326(-;-)
Make rs863225326(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112837777
GeneAPC
is asnp
is mentioned by
dbSNPrs863225326
dbSNP (old)rs863225326
ClinGenrs863225326
ebirs863225326
HLIrs863225326
Exacrs863225326
Gnomadrs863225326
Varsomers863225326
Maprs863225326
PheGenIrs863225326
Biobankrs863225326
1000 genomesrs863225326
hgdprs863225326
ensemblrs863225326
gopubmedrs863225326
geneviewrs863225326
scholarrs863225326
googlers863225326
pharmgkbrs863225326
gwascentralrs863225326
openSNPrs863225326
23andMers863225326
23andMe allrs863225326
SNP Nexus

SNPshotrs863225326
SNPdbers863225326
MSV3drs863225326
GWAS Ctlgrs863225326
Max Magnitude0
ClinVar
Risk rs863225326(-;-)
Alt rs863225326(-;-)
Reference Rs863225326(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112173474delA
CLNSRC
CLNACC RCV000202162.1,