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

rs863225353

From SNPedia

Orientationplus
Make rs863225353(-;-)
Make rs863225353(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112839760
GeneAPC
is asnp
is mentioned by
dbSNPrs863225353
ebirs863225353
HLIrs863225353
Exacrs863225353
Varsomers863225353
Maprs863225353
PheGenIrs863225353
hapmaprs863225353
1000 genomesrs863225353
hgdprs863225353
ensemblrs863225353
gopubmedrs863225353
geneviewrs863225353
scholarrs863225353
googlers863225353
pharmgkbrs863225353
gwascentralrs863225353
openSNPrs863225353
23andMers863225353
23andMe allrs863225353
SNP Nexus

SNPshotrs863225353
SNPdbers863225353
MSV3drs863225353
GWAS Ctlgrs863225353
Max Magnitude
ClinVar
Risk rs863225353(;)
Alt rs863225353(;)
Reference rs863225353(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112175457delC
CLNSRC
CLNACC RCV000202076.1,