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rs878853459

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs878853459(-;-)
Make rs878853459(-;G)
Make rs878853459(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112780853
GeneAPC
is asnp
is mentioned by
dbSNPrs878853459
ebirs878853459
HLIrs878853459
Exacrs878853459
Varsomers878853459
Maprs878853459
PheGenIrs878853459
hapmaprs878853459
1000 genomesrs878853459
hgdprs878853459
ensemblrs878853459
gopubmedrs878853459
geneviewrs878853459
scholarrs878853459
googlers878853459
pharmgkbrs878853459
gwascentralrs878853459
openSNPrs878853459
23andMers878853459
23andMe allrs878853459
SNP Nexus

SNPshotrs878853459
SNPdbers878853459
MSV3drs878853459
GWAS Ctlgrs878853459
Max Magnitude0
ClinVar
Risk rs878853459(G;G)
Alt rs878853459(G;G)
Reference rs878853459(;)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112116550dupG
CLNSRC
CLNACC RCV000232568.1,