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rs587782505

From SNPedia

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Geno Mag Summary
(TATC;TATC) 0 common in clinvar
Make rs587782505(-;-)
Make rs587782505(-;TATC)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112841965
GeneAPC
is asnp
is mentioned by
dbSNPrs587782505
ebirs587782505
HLIrs587782505
Exacrs587782505
Varsomers587782505
Maprs587782505
PheGenIrs587782505
hapmaprs587782505
1000 genomesrs587782505
hgdprs587782505
ensemblrs587782505
gopubmedrs587782505
geneviewrs587782505
scholarrs587782505
googlers587782505
pharmgkbrs587782505
gwascentralrs587782505
openSNPrs587782505
23andMers587782505
23andMe allrs587782505
SNP Nexus

SNPshotrs587782505
SNPdbers587782505
MSV3drs587782505
GWAS Ctlgrs587782505
Max Magnitude0
ClinVar
Risk rs587782505(;)
Alt rs587782505(;)
Reference rs587782505(TATC;TATC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112177662_112177665delTATC
CLNSRC
CLNACC RCV000131645.2,