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rs587779353

From SNPedia

Orientationplus
Geno Mag Summary
(CAAT;CAAT) 0 common in clinvar
Make rs587779353(-;-)
Make rs587779353(-;TCAA)
Make rs587779353(TCAA;TCAA)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112838796
GeneAPC
is asnp
is mentioned by
dbSNPrs587779353
ebirs587779353
HLIrs587779353
Exacrs587779353
Varsomers587779353
Maprs587779353
PheGenIrs587779353
hapmaprs587779353
1000 genomesrs587779353
hgdprs587779353
ensemblrs587779353
gopubmedrs587779353
geneviewrs587779353
scholarrs587779353
googlers587779353
pharmgkbrs587779353
gwascentralrs587779353
openSNPrs587779353
23andMers587779353
23andMe allrs587779353
SNP Nexus

SNPshotrs587779353
SNPdbers587779353
MSV3drs587779353
GWAS Ctlgrs587779353
Max Magnitude0
ClinVar
Risk rs587779353(;)
Alt rs587779353(;)
Reference rs587779353(CAAT;CAAT)
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.112174493_112174496delTCAA
CLNSRC GTR
CLNACC RCV000130649.2, RCV000201995.1, RCV000206027.1,