{{Rsnum
|rsid=2074409
|Gene=SYNRG
|Chromosome=17
|position=37538240
|Orientation=plus
|GMAF=0.3985
|Gene_s=SYNRG
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 54.9 | 37.2 | 8.0
| HCB | 16.8 | 56.2 | 27.0
| JPT | 12.4 | 47.8 | 39.8
| YRI | 21.1 | 53.1 | 25.9
| ASW | 26.8 | 58.9 | 14.3
| CHB | 16.8 | 56.2 | 27.0
| CHD | 12.8 | 44.0 | 43.1
| GIH | 47.5 | 42.6 | 9.9
| LWK | 19.1 | 47.3 | 33.6
| MEX | 55.2 | 36.2 | 8.6
| MKK | 39.7 | 47.4 | 12.8
| TSI | 71.6 | 23.5 | 4.9
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22566498
|Trait=None
|Title=Genomic association analysis identifies multiple loci influencing antihypertensive response to an angiotensin II receptor blocker.
|RiskAllele=T
|Pval=0.000002
|OR=1.2000
|ORtxt=None
|OA=1
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}