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

rs879253783

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs879253783(C;C)
Make rs879253783(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position112707527
GeneAPC
is asnp
is mentioned by
dbSNPrs879253783
ebirs879253783
HLIrs879253783
Exacrs879253783
Varsomers879253783
Maprs879253783
PheGenIrs879253783
hapmaprs879253783
1000 genomesrs879253783
hgdprs879253783
ensemblrs879253783
gopubmedrs879253783
geneviewrs879253783
scholarrs879253783
googlers879253783
pharmgkbrs879253783
gwascentralrs879253783
openSNPrs879253783
23andMers879253783
23andMe allrs879253783
SNP Nexus

SNPshotrs879253783
SNPdbers879253783
MSV3drs879253783
GWAS Ctlgrs879253783
Max Magnitude0
ClinVar
Risk rs879253783(C;C)
Alt rs879253783(C;C)
Reference rs879253783(T;T)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112043224T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000234996.1,