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rs863225335

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225335(G;T)
Make rs863225335(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112767269
GeneAPC
is asnp
is mentioned by
dbSNPrs863225335
ebirs863225335
HLIrs863225335
Exacrs863225335
Varsomers863225335
Maprs863225335
PheGenIrs863225335
hapmaprs863225335
1000 genomesrs863225335
hgdprs863225335
ensemblrs863225335
gopubmedrs863225335
geneviewrs863225335
scholarrs863225335
googlers863225335
pharmgkbrs863225335
gwascentralrs863225335
openSNPrs863225335
23andMers863225335
23andMe allrs863225335
SNP Nexus

SNPshotrs863225335
SNPdbers863225335
MSV3drs863225335
GWAS Ctlgrs863225335
Max Magnitude0
ClinVar
Risk rs863225335(T;T)
Alt rs863225335(T;T)
Reference rs863225335(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112102966G>T
CLNSRC
CLNACC RCV000202070.1,