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rs878853422

From SNPedia

Orientationplus
Geno Mag Summary
(AGTC;AGTC) 0 common in clinvar
Make rs878853422(-;-)
Make rs878853422(-;CAGT)
Make rs878853422(CAGT;CAGT)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112837625
GeneAPC
is asnp
is mentioned by
dbSNPrs878853422
ebirs878853422
HLIrs878853422
Exacrs878853422
Varsomers878853422
Maprs878853422
PheGenIrs878853422
hapmaprs878853422
1000 genomesrs878853422
hgdprs878853422
ensemblrs878853422
gopubmedrs878853422
geneviewrs878853422
scholarrs878853422
googlers878853422
pharmgkbrs878853422
gwascentralrs878853422
openSNPrs878853422
23andMers878853422
23andMe allrs878853422
SNP Nexus

SNPshotrs878853422
SNPdbers878853422
MSV3drs878853422
GWAS Ctlgrs878853422
Max Magnitude0
ClinVar
Risk rs878853422(;)
Alt rs878853422(;)
Reference rs878853422(AGTC;AGTC)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112173322_112173325delCAGT
CLNSRC
CLNACC RCV000230843.1,