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rs878853217

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878853217(-;-)
Make rs878853217(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112840311
GeneAPC
is asnp
is mentioned by
dbSNPrs878853217
ebirs878853217
HLIrs878853217
Exacrs878853217
Varsomers878853217
Maprs878853217
PheGenIrs878853217
hapmaprs878853217
1000 genomesrs878853217
hgdprs878853217
ensemblrs878853217
gopubmedrs878853217
geneviewrs878853217
scholarrs878853217
googlers878853217
pharmgkbrs878853217
gwascentralrs878853217
openSNPrs878853217
23andMers878853217
23andMe allrs878853217
SNP Nexus

SNPshotrs878853217
SNPdbers878853217
MSV3drs878853217
GWAS Ctlgrs878853217
Max Magnitude0
ClinVar
Risk rs878853217(;)
Alt rs878853217(;)
Reference rs878853217(G;G)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112176008delG
CLNSRC
CLNACC RCV000225339.1,