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rs11065611

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs11065611(C;T)
Make rs11065611(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position110266682
is asnp
is mentioned by
dbSNPrs11065611
ClinGenrs11065611
ebirs11065611
HLIrs11065611
Exacrs11065611
Varsomers11065611
Maprs11065611
PheGenIrs11065611
Biobankrs11065611
1000 genomesrs11065611
hgdprs11065611
ensemblrs11065611
gopubmedrs11065611
geneviewrs11065611
scholarrs11065611
googlers11065611
pharmgkbrs11065611
gwascentralrs11065611
openSNPrs11065611
23andMers11065611
23andMe allrs11065611
SNP Nexus

SNPshotrs11065611
SNPdbers11065611
MSV3drs11065611
GWAS Ctlgrs11065611
GMAF0.04178
Max Magnitude0
? (C;C) (C;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 9.9999999999999995E-8
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Alpha-1 globulin protein levels


GET Evidence
rs11065611
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.03125
summary