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rs863225317

From SNPedia

Orientationplus
Make rs863225317(-;-)
Make rs863225317(-;A)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112827989
GeneAPC
is asnp
is mentioned by
dbSNPrs863225317
ebirs863225317
HLIrs863225317
Exacrs863225317
Varsomers863225317
Maprs863225317
PheGenIrs863225317
hapmaprs863225317
1000 genomesrs863225317
hgdprs863225317
ensemblrs863225317
gopubmedrs863225317
geneviewrs863225317
scholarrs863225317
googlers863225317
pharmgkbrs863225317
gwascentralrs863225317
openSNPrs863225317
23andMers863225317
23andMe allrs863225317
SNP Nexus

SNPshotrs863225317
SNPdbers863225317
MSV3drs863225317
GWAS Ctlgrs863225317
Max Magnitude
ClinVar
Risk rs863225317(;)
Alt rs863225317(;)
Reference rs863225317(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112163686delA
CLNSRC
CLNACC RCV000201973.1,