Have questions? Visit https://www.reddit.com/r/SNPedia

rs878853438

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878853438(C;T)
Make rs878853438(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112838985
GeneAPC
is asnp
is mentioned by
dbSNPrs878853438
ebirs878853438
HLIrs878853438
Exacrs878853438
Varsomers878853438
Maprs878853438
PheGenIrs878853438
hapmaprs878853438
1000 genomesrs878853438
hgdprs878853438
ensemblrs878853438
gopubmedrs878853438
geneviewrs878853438
scholarrs878853438
googlers878853438
pharmgkbrs878853438
gwascentralrs878853438
openSNPrs878853438
23andMers878853438
23andMe allrs878853438
SNP Nexus

SNPshotrs878853438
SNPdbers878853438
MSV3drs878853438
GWAS Ctlgrs878853438
Max Magnitude0
ClinVar
Risk rs878853438(T;T)
Alt rs878853438(T;T)
Reference rs878853438(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.112174682C>T
CLNSRC
CLNACC RCV000231460.1,