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rs7112513

From SNPedia

Orientationplus
Stabilizedplus
Make rs7112513(A;A)
Make rs7112513(A;G)
Make rs7112513(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position117166645
GenePAFAH1B2
is asnp
is mentioned by
dbSNPrs7112513
ebirs7112513
HLIrs7112513
Exacrs7112513
Varsomers7112513
Maprs7112513
PheGenIrs7112513
hapmaprs7112513
1000 genomesrs7112513
hgdprs7112513
ensemblrs7112513
gopubmedrs7112513
geneviewrs7112513
scholarrs7112513
googlers7112513
pharmgkbrs7112513
gwascentralrs7112513
openSNPrs7112513
23andMers7112513
23andMe allrs7112513
SNP Nexus

SNPshotrs7112513
SNPdbers7112513
MSV3drs7112513
GWAS Ctlgrs7112513
GMAF0.2521
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 6E-9
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Soluble transferrin receptor protein levels


GET Evidence
rs7112513
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.78125
summary