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rs2729409

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2729409(A;A)
Make rs2729409(A;G)
ReferenceGRCh38 38.1/141
Chromosome18
Position30561722
is asnp
is mentioned by
dbSNPrs2729409
ebirs2729409
HLIrs2729409
Exacrs2729409
Varsomers2729409
Maprs2729409
PheGenIrs2729409
hapmaprs2729409
1000 genomesrs2729409
hgdprs2729409
ensemblrs2729409
gopubmedrs2729409
geneviewrs2729409
scholarrs2729409
googlers2729409
pharmgkbrs2729409
gwascentralrs2729409
openSNPrs2729409
23andMers2729409
23andMe allrs2729409
SNP Nexus

SNPshotrs2729409
SNPdbers2729409
MSV3drs2729409
GWAS Ctlgrs2729409
GMAF0.3072
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 0.0000030000000000000001
Odds Ratio NR NR

[PMID 18464913OA-icon.png] Parathyroid hormone (PTH) / parathormone protein levels


GET Evidence
rs2729409
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.351562
summary