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rs876658858

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658858(G;G)
Make rs876658858(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112828008
GeneAPC
is asnp
is mentioned by
dbSNPrs876658858
dbSNP (old)rs876658858
ClinGenrs876658858
ebirs876658858
HLIrs876658858
Exacrs876658858
Gnomadrs876658858
Varsomers876658858
Maprs876658858
PheGenIrs876658858
Biobankrs876658858
1000 genomesrs876658858
hgdprs876658858
ensemblrs876658858
gopubmedrs876658858
geneviewrs876658858
scholarrs876658858
googlers876658858
pharmgkbrs876658858
gwascentralrs876658858
openSNPrs876658858
23andMers876658858
23andMe allrs876658858
SNP Nexus

SNPshotrs876658858
SNPdbers876658858
MSV3drs876658858
GWAS Ctlgrs876658858
Max Magnitude0
ClinVar
Risk rs876658858(G;G)
Alt rs876658858(G;G)
Reference Rs876658858(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112163705T>G
CLNSRC
CLNACC RCV000215321.1,