Have questions? Visit https://www.reddit.com/r/SNPedia

rs863225337

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863225337(-;T)
Make rs863225337(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112838673
GeneAPC
is asnp
is mentioned by
dbSNPrs863225337
ClinGenrs863225337
ebirs863225337
HLIrs863225337
Exacrs863225337
Varsomers863225337
Maprs863225337
PheGenIrs863225337
hapmaprs863225337
1000 genomesrs863225337
hgdprs863225337
ensemblrs863225337
gopubmedrs863225337
geneviewrs863225337
scholarrs863225337
googlers863225337
pharmgkbrs863225337
gwascentralrs863225337
openSNPrs863225337
23andMers863225337
23andMe allrs863225337
SNP Nexus

SNPshotrs863225337
SNPdbers863225337
MSV3drs863225337
GWAS Ctlgrs863225337
Max Magnitude0
ClinVar
Risk rs863225337(T;T)
Alt rs863225337(T;T)
Reference Rs863225337(-;-)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112174370dupT
CLNSRC
CLNACC RCV000202266.1,