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rs509035

From SNPedia

Orientationplus
Stabilizedplus
Make rs509035(A;A)
Make rs509035(A;G)
Make rs509035(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position172445659
GeneGHSR
is asnp
is mentioned by
dbSNPrs509035
ebirs509035
HLIrs509035
Exacrs509035
Varsomers509035
Maprs509035
PheGenIrs509035
hapmaprs509035
1000 genomesrs509035
hgdprs509035
ensemblrs509035
gopubmedrs509035
geneviewrs509035
scholarrs509035
googlers509035
pharmgkbrs509035
gwascentralrs509035
openSNPrs509035
23andMers509035
23andMe allrs509035
SNP Nexus

SNPshotrs509035
SNPdbers509035
MSV3drs509035
GWAS Ctlgrs509035
GMAF0.2727
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 19593725OA-icon.png] Association of maternally inherited GNAS alleles with African-American male birth weight.


[PMID 20404923OA-icon.png] Family and population-based studies of variation within the ghrelin receptor locus in relation to measures of obesity.


[PMID 21269581] Analysis of the influence of the ghrelin receptor rs509035, rs512692 and rs2922126 polymorphisms in the risk of cardiovascular disease in patients with rheumatoid arthritis.


GET Evidence
rs509035
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.206349
summary