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rs863225342

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CATA;CATA) 0 common in clinvar
Make rs863225342(-;-)
Make rs863225342(-;TACA)
Make rs863225342(TACA;TACA)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112838898
GeneAPC
is asnp
is mentioned by
dbSNPrs863225342
dbSNP (old)rs863225342
ClinGenrs863225342
ebirs863225342
HLIrs863225342
Exacrs863225342
Varsomers863225342
Maprs863225342
PheGenIrs863225342
Biobankrs863225342
1000 genomesrs863225342
hgdprs863225342
ensemblrs863225342
gopubmedrs863225342
geneviewrs863225342
scholarrs863225342
googlers863225342
pharmgkbrs863225342
gwascentralrs863225342
openSNPrs863225342
23andMers863225342
23andMe allrs863225342
SNP Nexus

SNPshotrs863225342
SNPdbers863225342
MSV3drs863225342
GWAS Ctlgrs863225342
Max Magnitude0
ClinVar
Risk rs863225342(-;-)
Alt rs863225342(-;-)
Reference Rs863225342(CATA;CATA)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112174595_112174598delTACA
CLNSRC
CLNACC RCV000201986.1,