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rs587781330

From SNPedia

Orientationplus
Geno Mag Summary
(AAAC;AAAC) 0 common in clinvar
Make rs587781330(-;-)
Make rs587781330(-;AAAC)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112841528
GeneAPC
is asnp
is mentioned by
dbSNPrs587781330
ebirs587781330
HLIrs587781330
Exacrs587781330
Varsomers587781330
Maprs587781330
PheGenIrs587781330
hapmaprs587781330
1000 genomesrs587781330
hgdprs587781330
ensemblrs587781330
gopubmedrs587781330
geneviewrs587781330
scholarrs587781330
googlers587781330
pharmgkbrs587781330
gwascentralrs587781330
openSNPrs587781330
23andMers587781330
23andMe allrs587781330
SNP Nexus

SNPshotrs587781330
SNPdbers587781330
MSV3drs587781330
GWAS Ctlgrs587781330
Max Magnitude0
ClinVar
Risk rs587781330(;)
Alt rs587781330(;)
Reference rs587781330(AAAC;AAAC)
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.112177225_112177228delAAAC
CLNSRC
CLNACC RCV000129077.3, RCV000168219.3, RCV000202142.1,