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rs587781694

From SNPedia

Orientationplus
Geno Mag Summary
(AAAC;AAAC) 0 common in clinvar
Make rs587781694(-;-)
Make rs587781694(-;ACAA)
Make rs587781694(ACAA;ACAA)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112766337
GeneAPC
is asnp
is mentioned by
dbSNPrs587781694
ebirs587781694
HLIrs587781694
Exacrs587781694
Varsomers587781694
Maprs587781694
PheGenIrs587781694
hapmaprs587781694
1000 genomesrs587781694
hgdprs587781694
ensemblrs587781694
gopubmedrs587781694
geneviewrs587781694
scholarrs587781694
googlers587781694
pharmgkbrs587781694
gwascentralrs587781694
openSNPrs587781694
23andMers587781694
23andMe allrs587781694
SNP Nexus

SNPshotrs587781694
SNPdbers587781694
MSV3drs587781694
GWAS Ctlgrs587781694
Max Magnitude0
ClinVar
Risk rs587781694(;)
Alt rs587781694(;)
Reference rs587781694(AAAC;AAAC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112102034_112102037delACAA
CLNSRC
CLNACC RCV000129859.3,