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rs863225343

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225343(-;T)
Make rs863225343(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112839129
GeneAPC
is asnp
is mentioned by
dbSNPrs863225343
ClinGenrs863225343
ebirs863225343
HLIrs863225343
Exacrs863225343
Varsomers863225343
Maprs863225343
PheGenIrs863225343
hapmaprs863225343
1000 genomesrs863225343
hgdprs863225343
ensemblrs863225343
gopubmedrs863225343
geneviewrs863225343
scholarrs863225343
googlers863225343
pharmgkbrs863225343
gwascentralrs863225343
openSNPrs863225343
23andMers863225343
23andMe allrs863225343
SNP Nexus

SNPshotrs863225343
SNPdbers863225343
MSV3drs863225343
GWAS Ctlgrs863225343
Max Magnitude0
ClinVar
Risk rs863225343(T;T)
Alt rs863225343(T;T)
Reference Rs863225343(;)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112174826dupT
CLNSRC
CLNACC RCV000202129.1,