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rs4819143

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs4819143(A;A)
Make rs4819143(A;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position45704264
is asnp
is mentioned by
dbSNPrs4819143
ebirs4819143
HLIrs4819143
Exacrs4819143
Varsomers4819143
Maprs4819143
PheGenIrs4819143
hapmaprs4819143
1000 genomesrs4819143
hgdprs4819143
ensemblrs4819143
gopubmedrs4819143
geneviewrs4819143
scholarrs4819143
googlers4819143
pharmgkbrs4819143
gwascentralrs4819143
openSNPrs4819143
23andMers4819143
23andMe allrs4819143
SNP Nexus

SNPshotrs4819143
SNPdbers4819143
MSV3drs4819143
GWAS Ctlgrs4819143
GMAF0.1226
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21901158OA-icon.png]
Trait
Title Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.
Risk Allele C
P-val 0.000001
Odds Ratio 17.0000 [10.00 - 23.00] % decrease