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rs587781392

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587781392(C;T)
Make rs587781392(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112780895
GeneAPC
is asnp
is mentioned by
dbSNPrs587781392
ebirs587781392
HLIrs587781392
Exacrs587781392
Varsomers587781392
Maprs587781392
PheGenIrs587781392
hapmaprs587781392
1000 genomesrs587781392
hgdprs587781392
ensemblrs587781392
gopubmedrs587781392
geneviewrs587781392
scholarrs587781392
googlers587781392
pharmgkbrs587781392
gwascentralrs587781392
openSNPrs587781392
23andMers587781392
23andMe allrs587781392
SNP Nexus

SNPshotrs587781392
SNPdbers587781392
MSV3drs587781392
GWAS Ctlgrs587781392
Max Magnitude0
ClinVar
Risk rs587781392(T;T)
Alt rs587781392(T;T)
Reference rs587781392(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112116592C>T
CLNSRC
CLNACC RCV000129233.4, RCV000202175.1, RCV000227200.1,