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rs863225344

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863225344(C;T)
Make rs863225344(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112839282
GeneAPC
is asnp
is mentioned by
dbSNPrs863225344
ebirs863225344
HLIrs863225344
Exacrs863225344
Varsomers863225344
Maprs863225344
PheGenIrs863225344
hapmaprs863225344
1000 genomesrs863225344
hgdprs863225344
ensemblrs863225344
gopubmedrs863225344
geneviewrs863225344
scholarrs863225344
googlers863225344
pharmgkbrs863225344
gwascentralrs863225344
openSNPrs863225344
23andMers863225344
23andMe allrs863225344
SNP Nexus

SNPshotrs863225344
SNPdbers863225344
MSV3drs863225344
GWAS Ctlgrs863225344
Max Magnitude0
ClinVar
Risk rs863225344(T;T)
Alt rs863225344(T;T)
Reference rs863225344(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112174979C>T
CLNSRC
CLNACC RCV000202019.1,