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rs863225311

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225311(A;G)
Make rs863225311(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112819347
GeneAPC
is asnp
is mentioned by
dbSNPrs863225311
dbSNP (classic)rs863225311
ClinGenrs863225311
ebirs863225311
HLIrs863225311
Exacrs863225311
Gnomadrs863225311
Varsomers863225311
LitVarrs863225311
Maprs863225311
PheGenIrs863225311
Biobankrs863225311
1000 genomesrs863225311
hgdprs863225311
ensemblrs863225311
geneviewrs863225311
scholarrs863225311
googlers863225311
pharmgkbrs863225311
gwascentralrs863225311
openSNPrs863225311
23andMers863225311
SNPshotrs863225311
SNPdbers863225311
MSV3drs863225311
GWAS Ctlgrs863225311
Max Magnitude0
ClinVar
Risk rs863225311(G;G)
Alt rs863225311(G;G)
Reference Rs863225311(A;A)
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.112155044A>G
CLNSRC
CLNACC RCV000202161.1, RCV000204247.3, RCV000490831.1,