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rs863225357

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225357(C;T)
Make rs863225357(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112840239
GeneAPC
is asnp
is mentioned by
dbSNPrs863225357
ebirs863225357
HLIrs863225357
Exacrs863225357
Varsomers863225357
Maprs863225357
PheGenIrs863225357
hapmaprs863225357
1000 genomesrs863225357
hgdprs863225357
ensemblrs863225357
gopubmedrs863225357
geneviewrs863225357
scholarrs863225357
googlers863225357
pharmgkbrs863225357
gwascentralrs863225357
openSNPrs863225357
23andMers863225357
23andMe allrs863225357
SNP Nexus

SNPshotrs863225357
SNPdbers863225357
MSV3drs863225357
GWAS Ctlgrs863225357
Max Magnitude0
ClinVar
Risk rs863225357(T;T)
Alt rs863225357(T;T)
Reference rs863225357(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112175936C>T
CLNSRC
CLNACC RCV000202166.1,