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rs587783033

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587783033(-;-)
Make rs587783033(-;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112839408
GeneAPC
is asnp
is mentioned by
dbSNPrs587783033
ebirs587783033
HLIrs587783033
Exacrs587783033
Varsomers587783033
Maprs587783033
PheGenIrs587783033
hapmaprs587783033
1000 genomesrs587783033
hgdprs587783033
ensemblrs587783033
gopubmedrs587783033
geneviewrs587783033
scholarrs587783033
googlers587783033
pharmgkbrs587783033
gwascentralrs587783033
openSNPrs587783033
23andMers587783033
23andMe allrs587783033
SNP Nexus

SNPshotrs587783033
SNPdbers587783033
MSV3drs587783033
GWAS Ctlgrs587783033
Max Magnitude0
ClinVar
Risk rs587783033(;)
Alt rs587783033(;)
Reference rs587783033(T;T)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112175105delT
CLNSRC
CLNACC RCV000144569.1,