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rs863225310

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225310(A;A)
Make rs863225310(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112819345
GeneAPC
is asnp
is mentioned by
dbSNPrs863225310
dbSNP (classic)rs863225310
ClinGenrs863225310
ebirs863225310
HLIrs863225310
Exacrs863225310
Gnomadrs863225310
Varsomers863225310
LitVarrs863225310
Maprs863225310
PheGenIrs863225310
Biobankrs863225310
1000 genomesrs863225310
hgdprs863225310
ensemblrs863225310
geneviewrs863225310
scholarrs863225310
googlers863225310
pharmgkbrs863225310
gwascentralrs863225310
openSNPrs863225310
23andMers863225310
SNPshotrs863225310
SNPdbers863225310
MSV3drs863225310
GWAS Ctlgrs863225310
Max Magnitude0
ClinVar
Risk rs863225310(A;A)
Alt rs863225310(A;A)
Reference Rs863225310(G;G)
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.112155042G>A
CLNSRC
CLNACC RCV000202015.1, RCV000493121.1,