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rs587783031

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587783031(-;-)
Make rs587783031(-;A)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112840260
GeneAPC
is asnp
is mentioned by
dbSNPrs587783031
ebirs587783031
HLIrs587783031
Exacrs587783031
Varsomers587783031
Maprs587783031
PheGenIrs587783031
hapmaprs587783031
1000 genomesrs587783031
hgdprs587783031
ensemblrs587783031
gopubmedrs587783031
geneviewrs587783031
scholarrs587783031
googlers587783031
pharmgkbrs587783031
gwascentralrs587783031
openSNPrs587783031
23andMers587783031
23andMe allrs587783031
SNP Nexus

SNPshotrs587783031
SNPdbers587783031
MSV3drs587783031
GWAS Ctlgrs587783031
Max Magnitude0
ClinVar
Risk rs587783031(;)
Alt rs587783031(;)
Reference rs587783031(A;A)
Significance Pathogenic
Disease Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112175957delA
CLNSRC
CLNACC RCV000144566.1,