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rs587779786

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779786(A;T)
Make rs587779786(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112838682
GeneAPC
is asnp
is mentioned by
dbSNPrs587779786
ebirs587779786
HLIrs587779786
Exacrs587779786
Varsomers587779786
Maprs587779786
PheGenIrs587779786
hapmaprs587779786
1000 genomesrs587779786
hgdprs587779786
ensemblrs587779786
gopubmedrs587779786
geneviewrs587779786
scholarrs587779786
googlers587779786
pharmgkbrs587779786
gwascentralrs587779786
openSNPrs587779786
23andMers587779786
23andMe allrs587779786
SNP Nexus

SNPshotrs587779786
SNPdbers587779786
MSV3drs587779786
GWAS Ctlgrs587779786
Max Magnitude0
ClinVar
Risk rs587779786(T;T)
Alt rs587779786(T;T)
Reference rs587779786(A;A)
Significance Pathogenic
Disease not provided Familial adenomatous polyposis 1
Variation info
Gene APC
CLNDBN not provided Familial adenomatous polyposis 1
Reversed 0
HGVS NC_000005.9:g.112174379A>T
CLNSRC
CLNACC RCV000115077.2, RCV000174976.1,