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rs587781910

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587781910(-;-)
Make rs587781910(-;GTGTCAG)
Make rs587781910(GTGTCAG;GTGTCAG)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112838280
GeneAPC
is asnp
is mentioned by
dbSNPrs587781910
ebirs587781910
HLIrs587781910
Exacrs587781910
Varsomers587781910
Maprs587781910
PheGenIrs587781910
hapmaprs587781910
1000 genomesrs587781910
hgdprs587781910
ensemblrs587781910
gopubmedrs587781910
geneviewrs587781910
scholarrs587781910
googlers587781910
pharmgkbrs587781910
gwascentralrs587781910
openSNPrs587781910
23andMers587781910
23andMe allrs587781910
SNP Nexus

SNPshotrs587781910
SNPdbers587781910
MSV3drs587781910
GWAS Ctlgrs587781910
Max Magnitude0
ClinVar
Risk rs587781910(GTGTCAG;GTGTCAG)
Alt rs587781910(GTGTCAG;GTGTCAG)
Reference rs587781910(;)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome not provided
Reversed 0
HGVS NC_000005.9:g.112173971_112173977dupGTGTCAG
CLNSRC
CLNACC RCV000130251.2, RCV000236965.1,