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rs587782518

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587782518(C;T)
Make rs587782518(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112839810
GeneAPC
is asnp
is mentioned by
dbSNPrs587782518
ebirs587782518
HLIrs587782518
Exacrs587782518
Varsomers587782518
Maprs587782518
PheGenIrs587782518
hapmaprs587782518
1000 genomesrs587782518
hgdprs587782518
ensemblrs587782518
gopubmedrs587782518
geneviewrs587782518
scholarrs587782518
googlers587782518
pharmgkbrs587782518
gwascentralrs587782518
openSNPrs587782518
23andMers587782518
23andMe allrs587782518
SNP Nexus

SNPshotrs587782518
SNPdbers587782518
MSV3drs587782518
GWAS Ctlgrs587782518
Max Magnitude0
ClinVar
Risk rs587782518(G,T;G,T)
Alt rs587782518(G,T;G,T)
Reference rs587782518(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000005.9:g.112175507C>T
CLNSRC
CLNACC RCV000131673.2,