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rs863225350

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225350(-;TA)
Make rs863225350(TA;TA)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112839534
GeneAPC
is asnp
is mentioned by
dbSNPrs863225350
dbSNP (old)rs863225350
ClinGenrs863225350
ebirs863225350
HLIrs863225350
Exacrs863225350
Gnomadrs863225350
Varsomers863225350
Maprs863225350
PheGenIrs863225350
Biobankrs863225350
1000 genomesrs863225350
hgdprs863225350
ensemblrs863225350
gopubmedrs863225350
geneviewrs863225350
scholarrs863225350
googlers863225350
pharmgkbrs863225350
gwascentralrs863225350
openSNPrs863225350
23andMers863225350
23andMe allrs863225350
SNP Nexus

SNPshotrs863225350
SNPdbers863225350
MSV3drs863225350
GWAS Ctlgrs863225350
Max Magnitude0
ClinVar
Risk rs863225350(TA;TA)
Alt rs863225350(TA;TA)
Reference Rs863225350(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112175230_112175231dupTA
CLNSRC
CLNACC RCV000202296.1,