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rs587783029

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587783029(C;T)
Make rs587783029(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112838880
GeneAPC
is asnp
is mentioned by
dbSNPrs587783029
ebirs587783029
HLIrs587783029
Exacrs587783029
Varsomers587783029
Maprs587783029
PheGenIrs587783029
hapmaprs587783029
1000 genomesrs587783029
hgdprs587783029
ensemblrs587783029
gopubmedrs587783029
geneviewrs587783029
scholarrs587783029
googlers587783029
pharmgkbrs587783029
gwascentralrs587783029
openSNPrs587783029
23andMers587783029
23andMe allrs587783029
SNP Nexus

SNPshotrs587783029
SNPdbers587783029
MSV3drs587783029
GWAS Ctlgrs587783029
Max Magnitude0
ClinVar
Risk rs587783029(T;T)
Alt rs587783029(T;T)
Reference rs587783029(C;C)
Significance Pathogenic
Disease Familial adenomatous polyposis 1 not provided
Variation info
Gene APC
CLNDBN Familial adenomatous polyposis 1 not provided
Reversed 0
HGVS NC_000005.9:g.112174577C>T
CLNSRC
CLNACC RCV000144563.1, RCV000202095.1,