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rs878853432

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853432(C;G)
Make rs878853432(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112838389
GeneAPC
is asnp
is mentioned by
dbSNPrs878853432
ebirs878853432
HLIrs878853432
Exacrs878853432
Varsomers878853432
Maprs878853432
PheGenIrs878853432
hapmaprs878853432
1000 genomesrs878853432
hgdprs878853432
ensemblrs878853432
gopubmedrs878853432
geneviewrs878853432
scholarrs878853432
googlers878853432
pharmgkbrs878853432
gwascentralrs878853432
openSNPrs878853432
23andMers878853432
23andMe allrs878853432
SNP Nexus

SNPshotrs878853432
SNPdbers878853432
MSV3drs878853432
GWAS Ctlgrs878853432
Max Magnitude0
ClinVar
Risk rs878853432(G;G)
Alt rs878853432(G;G)
Reference rs878853432(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112174086C>G
CLNSRC
CLNACC RCV000225787.1,