Have questions? Visit https://www.reddit.com/r/SNPedia

rs863225366

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225366(C;T)
Make rs863225366(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112780799
GeneAPC
is asnp
is mentioned by
dbSNPrs863225366
ebirs863225366
HLIrs863225366
Exacrs863225366
Varsomers863225366
Maprs863225366
PheGenIrs863225366
hapmaprs863225366
1000 genomesrs863225366
hgdprs863225366
ensemblrs863225366
gopubmedrs863225366
geneviewrs863225366
scholarrs863225366
googlers863225366
pharmgkbrs863225366
gwascentralrs863225366
openSNPrs863225366
23andMers863225366
23andMe allrs863225366
SNP Nexus

SNPshotrs863225366
SNPdbers863225366
MSV3drs863225366
GWAS Ctlgrs863225366
Max Magnitude0
ClinVar
Risk rs863225366(T;T)
Alt rs863225366(T;T)
Reference rs863225366(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112116496C>T
CLNSRC
CLNACC RCV000201966.1,