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rs863225332

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(-;-) 0 common/normal
(-;A) 4 linked to certain hereditary cancers
Make rs863225332(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112838398
GeneAPC
is asnp
is mentioned by
dbSNPrs863225332
dbSNP (old)rs863225332
ClinGenrs863225332
ebirs863225332
HLIrs863225332
Exacrs863225332
Gnomadrs863225332
Varsomers863225332
Maprs863225332
PheGenIrs863225332
Biobankrs863225332
1000 genomesrs863225332
hgdprs863225332
ensemblrs863225332
gopubmedrs863225332
geneviewrs863225332
scholarrs863225332
googlers863225332
pharmgkbrs863225332
gwascentralrs863225332
openSNPrs863225332
23andMers863225332
23andMe allrs863225332
SNP Nexus

SNPshotrs863225332
SNPdbers863225332
MSV3drs863225332
GWAS Ctlgrs863225332
Max Magnitude4
ClinVar
Risk rs863225332(A;A)
Alt rs863225332(A;A)
Reference Rs863225332(-;-)
Significance Pathogenic
Disease not provided Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN not provided Familial adenomatous polyposis 1 Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112174095dupA
CLNSRC
CLNACC RCV000202260.1, RCV000410020.1, RCV000490899.1,