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rs2066219

From SNPedia

Orientationminus
Stabilizedplus
Make rs2066219(C;C)
Make rs2066219(C;T)
Make rs2066219(T;T)
ReferenceGRCh38 38.1/142
Chromosome13
Position68956532
is asnp
is mentioned by
dbSNPrs2066219
ebirs2066219
HLIrs2066219
Exacrs2066219
Varsomers2066219
Maprs2066219
PheGenIrs2066219
hapmaprs2066219
1000 genomesrs2066219
hgdprs2066219
ensemblrs2066219
gopubmedrs2066219
geneviewrs2066219
scholarrs2066219
googlers2066219
pharmgkbrs2066219
gwascentralrs2066219
openSNPrs2066219
23andMers2066219
23andMe allrs2066219
SNP Nexus

SNPshotrs2066219
SNPdbers2066219
MSV3drs2066219
GWAS Ctlgrs2066219
GMAF0.2713
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 17903298OA-icon.png]
Trait Diabetes related insulin traits
Title Genome-wide association with diabetes-related traits in the Framingham Heart Study
Risk Allele
P-val 0.0000090000000000000002
Odds Ratio NR NR


GET Evidence
rs2066219
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.698413
summary