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rs863225352

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863225352(A;T)
Make rs863225352(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112839669
GeneAPC
is asnp
is mentioned by
dbSNPrs863225352
ebirs863225352
HLIrs863225352
Exacrs863225352
Varsomers863225352
Maprs863225352
PheGenIrs863225352
hapmaprs863225352
1000 genomesrs863225352
hgdprs863225352
ensemblrs863225352
gopubmedrs863225352
geneviewrs863225352
scholarrs863225352
googlers863225352
pharmgkbrs863225352
gwascentralrs863225352
openSNPrs863225352
23andMers863225352
23andMe allrs863225352
SNP Nexus

SNPshotrs863225352
SNPdbers863225352
MSV3drs863225352
GWAS Ctlgrs863225352
Max Magnitude0
ClinVar
Risk rs863225352(T;T)
Alt rs863225352(T;T)
Reference rs863225352(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112175366A>T
CLNSRC
CLNACC RCV000202280.1,