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rs876658325

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658325(C;T)
Make rs876658325(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112775687
GeneAPC
is asnp
is mentioned by
dbSNPrs876658325
ClinGenrs876658325
ebirs876658325
HLIrs876658325
Exacrs876658325
Varsomers876658325
Maprs876658325
PheGenIrs876658325
hapmaprs876658325
1000 genomesrs876658325
hgdprs876658325
ensemblrs876658325
gopubmedrs876658325
geneviewrs876658325
scholarrs876658325
googlers876658325
pharmgkbrs876658325
gwascentralrs876658325
openSNPrs876658325
23andMers876658325
23andMe allrs876658325
SNP Nexus

SNPshotrs876658325
SNPdbers876658325
MSV3drs876658325
GWAS Ctlgrs876658325
Max Magnitude0
ClinVar
Risk rs876658325(T;T)
Alt rs876658325(T;T)
Reference Rs876658325(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112111384C>T
CLNSRC
CLNACC RCV000221156.1,