Have questions? Visit https://www.reddit.com/r/SNPedia

rs169082

From SNPedia

Orientationminus
Stabilizedminus
Make rs169082(A;A)
Make rs169082(A;G)
Make rs169082(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position169647052
GeneDOCK2
is asnp
is mentioned by
dbSNPrs169082
ebirs169082
HLIrs169082
Exacrs169082
Varsomers169082
Maprs169082
PheGenIrs169082
hapmaprs169082
1000 genomesrs169082
hgdprs169082
ensemblrs169082
gopubmedrs169082
geneviewrs169082
scholarrs169082
googlers169082
pharmgkbrs169082
gwascentralrs169082
openSNPrs169082
23andMers169082
23andMe allrs169082
SNP Nexus

SNPshotrs169082
SNPdbers169082
MSV3drs169082
GWAS Ctlgrs169082
GMAF0.4394
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 18464913OA-icon.png]
Trait Protein quantitative trait loci
Title A Genome-Wide Association Study Identifies Protein Quantitative Trait Loci (pQTLs)
Risk Allele
P-val 9.9999999999999995E-7
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Leptin (LEP) protein levels


GET Evidence
rs169082
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.484127
summary