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rs863225372

From SNPedia

Orientationplus
Make rs863225372(-;-)
Make rs863225372(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112801349
GeneAPC
is asnp
is mentioned by
dbSNPrs863225372
ebirs863225372
HLIrs863225372
Exacrs863225372
Varsomers863225372
Maprs863225372
PheGenIrs863225372
hapmaprs863225372
1000 genomesrs863225372
hgdprs863225372
ensemblrs863225372
gopubmedrs863225372
geneviewrs863225372
scholarrs863225372
googlers863225372
pharmgkbrs863225372
gwascentralrs863225372
openSNPrs863225372
23andMers863225372
23andMe allrs863225372
SNP Nexus

SNPshotrs863225372
SNPdbers863225372
MSV3drs863225372
GWAS Ctlgrs863225372
Max Magnitude
ClinVar
Risk rs863225372(;)
Alt rs863225372(;)
Reference rs863225372(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112137046delG
CLNSRC
CLNACC RCV000202132.1,