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rs587782303

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782303(-;-)
Make rs587782303(-;C)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112837598
GeneAPC
is asnp
is mentioned by
dbSNPrs587782303
ebirs587782303
HLIrs587782303
Exacrs587782303
Varsomers587782303
Maprs587782303
PheGenIrs587782303
hapmaprs587782303
1000 genomesrs587782303
hgdprs587782303
ensemblrs587782303
gopubmedrs587782303
geneviewrs587782303
scholarrs587782303
googlers587782303
pharmgkbrs587782303
gwascentralrs587782303
openSNPrs587782303
23andMers587782303
23andMe allrs587782303
SNP Nexus

SNPshotrs587782303
SNPdbers587782303
MSV3drs587782303
GWAS Ctlgrs587782303
Max Magnitude0
ClinVar
Risk rs587782303(;)
Alt rs587782303(;)
Reference rs587782303(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1 not provided
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1 not provided
Reversed 0
HGVS NC_000005.9:g.112173295delC
CLNSRC
CLNACC RCV000131187.4, RCV000197295.2, RCV000211899.1,