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rs863225368

From SNPedia

Orientationplus
Make rs863225368(-;-)
Make rs863225368(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112841530
GeneAPC
is asnp
is mentioned by
dbSNPrs863225368
ebirs863225368
HLIrs863225368
Exacrs863225368
Varsomers863225368
Maprs863225368
PheGenIrs863225368
hapmaprs863225368
1000 genomesrs863225368
hgdprs863225368
ensemblrs863225368
gopubmedrs863225368
geneviewrs863225368
scholarrs863225368
googlers863225368
pharmgkbrs863225368
gwascentralrs863225368
openSNPrs863225368
23andMers863225368
23andMe allrs863225368
SNP Nexus

SNPshotrs863225368
SNPdbers863225368
MSV3drs863225368
GWAS Ctlgrs863225368
Max Magnitude
ClinVar
Risk rs863225368(;)
Alt rs863225368(;)
Reference rs863225368(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112177227delA
CLNSRC
CLNACC RCV000202237.1,