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rs587782293

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587782293(A;A)
Make rs587782293(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112775626
GeneAPC
is asnp
is mentioned by
dbSNPrs587782293
ebirs587782293
HLIrs587782293
Exacrs587782293
Varsomers587782293
Maprs587782293
PheGenIrs587782293
hapmaprs587782293
1000 genomesrs587782293
hgdprs587782293
ensemblrs587782293
gopubmedrs587782293
geneviewrs587782293
scholarrs587782293
googlers587782293
pharmgkbrs587782293
gwascentralrs587782293
openSNPrs587782293
23andMers587782293
23andMe allrs587782293
SNP Nexus

SNPshotrs587782293
SNPdbers587782293
MSV3drs587782293
GWAS Ctlgrs587782293
Max Magnitude0
ClinVar
Risk rs587782293(A;A)
Alt rs587782293(A;A)
Reference rs587782293(T;T)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not specified
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome not specified
Reversed 0
HGVS NC_000005.9:g.112111323T>A
CLNSRC
CLNACC RCV000131175.2, RCV000202091.1,