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

rs4742971

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common on affy axiom data
Make rs4742971(G;T)
Make rs4742971(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position105892815
is asnp
is mentioned by
dbSNPrs4742971
ebirs4742971
HLIrs4742971
Exacrs4742971
Varsomers4742971
Maprs4742971
PheGenIrs4742971
hapmaprs4742971
1000 genomesrs4742971
hgdprs4742971
ensemblrs4742971
gopubmedrs4742971
geneviewrs4742971
scholarrs4742971
googlers4742971
pharmgkbrs4742971
gwascentralrs4742971
openSNPrs4742971
23andMers4742971
23andMe allrs4742971
SNP Nexus

SNPshotrs4742971
SNPdbers4742971
MSV3drs4742971
GWAS Ctlgrs4742971
GMAF0.1892
Max Magnitude0
? (G;G) (G;T) (T;T) 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 7.9999999999999996E-7
Odds Ratio NR NR

[PMID 18464913OA-icon.png] GPT (ALT) protein levels


GET Evidence
rs4742971
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary