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rs863225330

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225330(-;A)
Make rs863225330(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112838218
GeneAPC
is asnp
is mentioned by
dbSNPrs863225330
dbSNP (old)rs863225330
ClinGenrs863225330
ebirs863225330
HLIrs863225330
Exacrs863225330
Gnomadrs863225330
Varsomers863225330
Maprs863225330
PheGenIrs863225330
Biobankrs863225330
1000 genomesrs863225330
hgdprs863225330
ensemblrs863225330
gopubmedrs863225330
geneviewrs863225330
scholarrs863225330
googlers863225330
pharmgkbrs863225330
gwascentralrs863225330
openSNPrs863225330
23andMers863225330
23andMe allrs863225330
SNP Nexus

SNPshotrs863225330
SNPdbers863225330
MSV3drs863225330
GWAS Ctlgrs863225330
Max Magnitude0
ClinVar
Risk rs863225330(A;A)
Alt rs863225330(A;A)
Reference Rs863225330(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112173915dupA
CLNSRC
CLNACC RCV000202233.1,