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rs863225346

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225346(-;T)
Make rs863225346(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112839385
GeneAPC
is asnp
is mentioned by
dbSNPrs863225346
dbSNP (old)rs863225346
ClinGenrs863225346
ebirs863225346
HLIrs863225346
Exacrs863225346
Gnomadrs863225346
Varsomers863225346
Maprs863225346
PheGenIrs863225346
Biobankrs863225346
1000 genomesrs863225346
hgdprs863225346
ensemblrs863225346
gopubmedrs863225346
geneviewrs863225346
scholarrs863225346
googlers863225346
pharmgkbrs863225346
gwascentralrs863225346
openSNPrs863225346
23andMers863225346
23andMe allrs863225346
SNP Nexus

SNPshotrs863225346
SNPdbers863225346
MSV3drs863225346
GWAS Ctlgrs863225346
Max Magnitude0
ClinVar
Risk rs863225346(T;T)
Alt rs863225346(T;T)
Reference Rs863225346(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112175082dupT
CLNSRC
CLNACC RCV000202254.1,