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rs878853444

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853444(A;T)
Make rs878853444(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112775654
GeneAPC
is asnp
is mentioned by
dbSNPrs878853444
ebirs878853444
HLIrs878853444
Exacrs878853444
Varsomers878853444
Maprs878853444
PheGenIrs878853444
hapmaprs878853444
1000 genomesrs878853444
hgdprs878853444
ensemblrs878853444
gopubmedrs878853444
geneviewrs878853444
scholarrs878853444
googlers878853444
pharmgkbrs878853444
gwascentralrs878853444
openSNPrs878853444
23andMers878853444
23andMe allrs878853444
SNP Nexus

SNPshotrs878853444
SNPdbers878853444
MSV3drs878853444
GWAS Ctlgrs878853444
Max Magnitude0
ClinVar
Risk rs878853444(T;T)
Alt rs878853444(T;T)
Reference rs878853444(A;A)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112111351A>T
CLNSRC
CLNACC RCV000231021.1,