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rs863225369

From SNPedia

Orientationplus
Make rs863225369(-;-)
Make rs863225369(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112841590
GeneAPC
is asnp
is mentioned by
dbSNPrs863225369
ebirs863225369
HLIrs863225369
Exacrs863225369
Varsomers863225369
Maprs863225369
PheGenIrs863225369
hapmaprs863225369
1000 genomesrs863225369
hgdprs863225369
ensemblrs863225369
gopubmedrs863225369
geneviewrs863225369
scholarrs863225369
googlers863225369
pharmgkbrs863225369
gwascentralrs863225369
openSNPrs863225369
23andMers863225369
23andMe allrs863225369
SNP Nexus

SNPshotrs863225369
SNPdbers863225369
MSV3drs863225369
GWAS Ctlgrs863225369
Max Magnitude
ClinVar
Risk rs863225369(;)
Alt rs863225369(;)
Reference rs863225369(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112177287delC
CLNSRC
CLNACC RCV000202028.1,