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rs4541776

From SNPedia

Orientationplus
Stabilizedplus
Make rs4541776(A;A)
Make rs4541776(A;G)
Make rs4541776(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position121581723
is asnp
is mentioned by
dbSNPrs4541776
ebirs4541776
HLIrs4541776
Exacrs4541776
Varsomers4541776
Maprs4541776
PheGenIrs4541776
hapmaprs4541776
1000 genomesrs4541776
hgdprs4541776
ensemblrs4541776
gopubmedrs4541776
geneviewrs4541776
scholarrs4541776
googlers4541776
pharmgkbrs4541776
gwascentralrs4541776
openSNPrs4541776
23andMers4541776
23andMe allrs4541776
SNP Nexus

SNPshotrs4541776
SNPdbers4541776
MSV3drs4541776
GWAS Ctlgrs4541776
GMAF0.365
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 0.0000019999999999999999
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Gamma-glutamyl transpeptidase / Gamma-glutamyltransferase (GGT) protein levels


GET Evidence
rs4541776
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency
summary