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rs878853436

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853436(-;-)
Make rs878853436(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112838790
GeneAPC
is asnp
is mentioned by
dbSNPrs878853436
dbSNP (classic)rs878853436
ClinGenrs878853436
ebirs878853436
HLIrs878853436
Exacrs878853436
Gnomadrs878853436
Varsomers878853436
LitVarrs878853436
Maprs878853436
PheGenIrs878853436
Biobankrs878853436
1000 genomesrs878853436
hgdprs878853436
ensemblrs878853436
geneviewrs878853436
scholarrs878853436
googlers878853436
pharmgkbrs878853436
gwascentralrs878853436
openSNPrs878853436
23andMers878853436
SNPshotrs878853436
SNPdbers878853436
MSV3drs878853436
GWAS Ctlgrs878853436
Max Magnitude0
ClinVar
Risk rs878853436(-;-)
Alt rs878853436(-;-)
Reference Rs878853436(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.112174487delA
CLNSRC
CLNACC RCV000227841.1,