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rs490683

From SNPedia

Orientationplus
Stabilizedplus
Make rs490683(C;C)
Make rs490683(C;G)
Make rs490683(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position172457284
is asnp
is mentioned by
dbSNPrs490683
ebirs490683
HLIrs490683
Exacrs490683
Varsomers490683
Maprs490683
PheGenIrs490683
hapmaprs490683
1000 genomesrs490683
hgdprs490683
ensemblrs490683
gopubmedrs490683
geneviewrs490683
scholarrs490683
googlers490683
pharmgkbrs490683
gwascentralrs490683
openSNPrs490683
23andMers490683
23andMe allrs490683
SNP Nexus

SNPshotrs490683
SNPdbers490683
MSV3drs490683
GWAS Ctlgrs490683
GMAF0.2902
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 22411573OA-icon.png] Association of ghrelin receptor promoter polymorphisms with weight loss following Roux-en-Y gastric bypass surgery.


GET Evidence
rs490683
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.3125
summary