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rs587779790

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587779790(A;T)
Make rs587779790(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position112839066
GeneAPC
is asnp
is mentioned by
dbSNPrs587779790
ebirs587779790
HLIrs587779790
Exacrs587779790
Varsomers587779790
Maprs587779790
PheGenIrs587779790
hapmaprs587779790
1000 genomesrs587779790
hgdprs587779790
ensemblrs587779790
gopubmedrs587779790
geneviewrs587779790
scholarrs587779790
googlers587779790
pharmgkbrs587779790
gwascentralrs587779790
openSNPrs587779790
23andMers587779790
23andMe allrs587779790
SNP Nexus

SNPshotrs587779790
SNPdbers587779790
MSV3drs587779790
GWAS Ctlgrs587779790
Max Magnitude0
ClinVar
Risk rs587779790(T;T)
Alt rs587779790(T;T)
Reference rs587779790(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene APC
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.112174763A>T
CLNSRC
CLNACC RCV000115085.3,