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rs755046558

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs755046558(A;A)
Make rs755046558(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position112843105
GeneAPC
is asnp
is mentioned by
dbSNPrs755046558
ebirs755046558
HLIrs755046558
Exacrs755046558
Varsomers755046558
Maprs755046558
PheGenIrs755046558
hapmaprs755046558
1000 genomesrs755046558
hgdprs755046558
ensemblrs755046558
gopubmedrs755046558
geneviewrs755046558
scholarrs755046558
googlers755046558
pharmgkbrs755046558
gwascentralrs755046558
openSNPrs755046558
23andMers755046558
23andMe allrs755046558
SNP Nexus

SNPshotrs755046558
SNPdbers755046558
MSV3drs755046558
GWAS Ctlgrs755046558
Max Magnitude0
ClinVar
Risk rs755046558(A;A)
Alt rs755046558(A;A)
Reference rs755046558(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112178802G>A
CLNSRC
CLNACC RCV000201984.1,