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rs7043482

From SNPedia

Orientationplus
Stabilizedplus
Make rs7043482(A;A)
Make rs7043482(A;C)
Make rs7043482(C;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position82521000
is asnp
is mentioned by
dbSNPrs7043482
ebirs7043482
HLIrs7043482
Exacrs7043482
Varsomers7043482
Maprs7043482
PheGenIrs7043482
hapmaprs7043482
1000 genomesrs7043482
hgdprs7043482
ensemblrs7043482
gopubmedrs7043482
geneviewrs7043482
scholarrs7043482
googlers7043482
pharmgkbrs7043482
gwascentralrs7043482
openSNPrs7043482
23andMers7043482
23andMe allrs7043482
SNP Nexus

SNPshotrs7043482
SNPdbers7043482
MSV3drs7043482
GWAS Ctlgrs7043482
GMAF0.4573
Max Magnitude
? (A;A) (A;C) (C;C) 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 G
P-val 0.000003
Odds Ratio 12.0000 [7.00 - 18.00] % increase


[PMID 17434096OA-icon.png] A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release.