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rs863225308

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225308(-;T)
Make rs863225308(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112819261
GeneAPC
is asnp
is mentioned by
dbSNPrs863225308
dbSNP (old)rs863225308
ClinGenrs863225308
ebirs863225308
HLIrs863225308
Exacrs863225308
Gnomadrs863225308
Varsomers863225308
Maprs863225308
PheGenIrs863225308
Biobankrs863225308
1000 genomesrs863225308
hgdprs863225308
ensemblrs863225308
gopubmedrs863225308
geneviewrs863225308
scholarrs863225308
googlers863225308
pharmgkbrs863225308
gwascentralrs863225308
openSNPrs863225308
23andMers863225308
23andMe allrs863225308
SNP Nexus

SNPshotrs863225308
SNPdbers863225308
MSV3drs863225308
GWAS Ctlgrs863225308
Max Magnitude0
ClinVar
Risk rs863225308(T;T)
Alt rs863225308(T;T)
Reference Rs863225308(-;-)
Significance Pathogenic
Disease not provided Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN not provided Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112154958dupT
CLNSRC
CLNACC RCV000202239.1, RCV000491236.1,