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rs587779783

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587779783(C;T)
Make rs587779783(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112838007
GeneAPC
is asnp
is mentioned by
dbSNPrs587779783
ebirs587779783
HLIrs587779783
Exacrs587779783
Varsomers587779783
Maprs587779783
PheGenIrs587779783
hapmaprs587779783
1000 genomesrs587779783
hgdprs587779783
ensemblrs587779783
gopubmedrs587779783
geneviewrs587779783
scholarrs587779783
googlers587779783
pharmgkbrs587779783
gwascentralrs587779783
openSNPrs587779783
23andMers587779783
23andMe allrs587779783
SNP Nexus

SNPshotrs587779783
SNPdbers587779783
MSV3drs587779783
GWAS Ctlgrs587779783
Max Magnitude0
ClinVar
Risk rs587779783(G,T;G,T)
Alt rs587779783(G,T;G,T)
Reference rs587779783(C;C)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1 Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene APC
CLNDBN Hereditary cancer-predisposing syndrome Familial adenomatous polyposis 1 Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000005.9:g.112173704C>G; NC_000005.9:g.112173704C>T
CLNSRC
CLNACC RCV000129231.2, RCV000115073.2, RCV000168336.2, RCV000222493.1,