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rs863225371

From SNPedia

Orientationplus
Make rs863225371(-;-)
Make rs863225371(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112792477
GeneAPC
is asnp
is mentioned by
dbSNPrs863225371
ebirs863225371
HLIrs863225371
Exacrs863225371
Varsomers863225371
Maprs863225371
PheGenIrs863225371
hapmaprs863225371
1000 genomesrs863225371
hgdprs863225371
ensemblrs863225371
gopubmedrs863225371
geneviewrs863225371
scholarrs863225371
googlers863225371
pharmgkbrs863225371
gwascentralrs863225371
openSNPrs863225371
23andMers863225371
23andMe allrs863225371
SNP Nexus

SNPshotrs863225371
SNPdbers863225371
MSV3drs863225371
GWAS Ctlgrs863225371
Max Magnitude
ClinVar
Risk rs863225371(;)
Alt rs863225371(;)
Reference rs863225371(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112128174delA
CLNSRC
CLNACC RCV000202065.1,