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

rs16957063

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs16957063(A;G)
Make rs16957063(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position42692090
GeneSTARD9
is asnp
is mentioned by
dbSNPrs16957063
ebirs16957063
HLIrs16957063
Exacrs16957063
Varsomers16957063
Maprs16957063
PheGenIrs16957063
hapmaprs16957063
1000 genomesrs16957063
hgdprs16957063
ensemblrs16957063
gopubmedrs16957063
geneviewrs16957063
scholarrs16957063
googlers16957063
pharmgkbrs16957063
gwascentralrs16957063
openSNPrs16957063
23andMers16957063
23andMe allrs16957063
SNP Nexus

SNPshotrs16957063
SNPdbers16957063
MSV3drs16957063
GWAS Ctlgrs16957063
GMAF0.07713
Max Magnitude0
? (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 4.9999999999999998E-7
Odds Ratio NR NR

[PMID 18464913OA-icon.png] free thyroxine / T4 / T4 (Ft4) protein levels


GET Evidence
rs16957063
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0377242
summary