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rs587782744

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782744(-;-)
Make rs587782744(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112819133
GeneAPC
is asnp
is mentioned by
dbSNPrs587782744
ebirs587782744
HLIrs587782744
Exacrs587782744
Varsomers587782744
Maprs587782744
PheGenIrs587782744
hapmaprs587782744
1000 genomesrs587782744
hgdprs587782744
ensemblrs587782744
gopubmedrs587782744
geneviewrs587782744
scholarrs587782744
googlers587782744
pharmgkbrs587782744
gwascentralrs587782744
openSNPrs587782744
23andMers587782744
23andMe allrs587782744
SNP Nexus

SNPshotrs587782744
SNPdbers587782744
MSV3drs587782744
GWAS Ctlgrs587782744
Max Magnitude0
ClinVar
Risk rs587782744(;)
Alt rs587782744(;)
Reference rs587782744(T;T)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112154830delT
CLNSRC
CLNACC RCV000132249.2,