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rs878853449

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs878853449(-;-)
Make rs878853449(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112840295
GeneAPC
is asnp
is mentioned by
dbSNPrs878853449
ebirs878853449
HLIrs878853449
Exacrs878853449
Varsomers878853449
Maprs878853449
PheGenIrs878853449
hapmaprs878853449
1000 genomesrs878853449
hgdprs878853449
ensemblrs878853449
gopubmedrs878853449
geneviewrs878853449
scholarrs878853449
googlers878853449
pharmgkbrs878853449
gwascentralrs878853449
openSNPrs878853449
23andMers878853449
23andMe allrs878853449
SNP Nexus

SNPshotrs878853449
SNPdbers878853449
MSV3drs878853449
GWAS Ctlgrs878853449
Max Magnitude0
ClinVar
Risk rs878853449(;)
Alt rs878853449(;)
Reference rs878853449(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.112175992delA
CLNSRC
CLNACC RCV000228486.1,