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rs863225334

From SNPedia

Orientationplus
Make rs863225334(-;-)
Make rs863225334(-;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112838480
GeneAPC
is asnp
is mentioned by
dbSNPrs863225334
ebirs863225334
HLIrs863225334
Exacrs863225334
Varsomers863225334
Maprs863225334
PheGenIrs863225334
hapmaprs863225334
1000 genomesrs863225334
hgdprs863225334
ensemblrs863225334
gopubmedrs863225334
geneviewrs863225334
scholarrs863225334
googlers863225334
pharmgkbrs863225334
gwascentralrs863225334
openSNPrs863225334
23andMers863225334
23andMe allrs863225334
SNP Nexus

SNPshotrs863225334
SNPdbers863225334
MSV3drs863225334
GWAS Ctlgrs863225334
Max Magnitude
ClinVar
Risk rs863225334(;)
Alt rs863225334(;)
Reference rs863225334(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112174177delT
CLNSRC
CLNACC RCV000202041.1,