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rs587781809

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587781809(A;A)
Make rs587781809(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112766412
GeneAPC
is asnp
is mentioned by
dbSNPrs587781809
ebirs587781809
HLIrs587781809
Exacrs587781809
Varsomers587781809
Maprs587781809
PheGenIrs587781809
hapmaprs587781809
1000 genomesrs587781809
hgdprs587781809
ensemblrs587781809
gopubmedrs587781809
geneviewrs587781809
scholarrs587781809
googlers587781809
pharmgkbrs587781809
gwascentralrs587781809
openSNPrs587781809
23andMers587781809
23andMe allrs587781809
SNP Nexus

SNPshotrs587781809
SNPdbers587781809
MSV3drs587781809
GWAS Ctlgrs587781809
Max Magnitude0
ClinVar
Risk rs587781809(A;A)
Alt rs587781809(A;A)
Reference rs587781809(T;T)
Significance Probable-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.112102109T>A
CLNSRC
CLNACC RCV000130080.2, RCV000202191.1, RCV000231290.1,