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

rs587779780

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779780(C;T)
Make rs587779780(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112819245
GeneAPC
is asnp
is mentioned by
dbSNPrs587779780
ebirs587779780
HLIrs587779780
Exacrs587779780
Varsomers587779780
Maprs587779780
PheGenIrs587779780
hapmaprs587779780
1000 genomesrs587779780
hgdprs587779780
ensemblrs587779780
gopubmedrs587779780
geneviewrs587779780
scholarrs587779780
googlers587779780
pharmgkbrs587779780
gwascentralrs587779780
openSNPrs587779780
23andMers587779780
23andMe allrs587779780
SNP Nexus

SNPshotrs587779780
SNPdbers587779780
MSV3drs587779780
GWAS Ctlgrs587779780
Max Magnitude0
ClinVar
Risk rs587779780(T;T)
Alt rs587779780(T;T)
Reference rs587779780(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112154942C>T
CLNSRC
CLNACC RCV000115066.5, RCV000202096.1, RCV000234357.1,