Have questions? Visit https://www.reddit.com/r/SNPedia

rs879253784

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs879253784(A;G)
Make rs879253784(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112707526
GeneAPC
is asnp
is mentioned by
dbSNPrs879253784
ebirs879253784
HLIrs879253784
Exacrs879253784
Varsomers879253784
Maprs879253784
PheGenIrs879253784
hapmaprs879253784
1000 genomesrs879253784
hgdprs879253784
ensemblrs879253784
gopubmedrs879253784
geneviewrs879253784
scholarrs879253784
googlers879253784
pharmgkbrs879253784
gwascentralrs879253784
openSNPrs879253784
23andMers879253784
23andMe allrs879253784
SNP Nexus

SNPshotrs879253784
SNPdbers879253784
MSV3drs879253784
GWAS Ctlgrs879253784
Max Magnitude0
ClinVar
Risk rs879253784(G,T;G,T)
Alt rs879253784(G,T;G,T)
Reference rs879253784(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.112043223A>G; NC_000005.9:g.112043223A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000234977.1, RCV000234988.1,