{{Rsnum
|rsid=1880753
|Gene=CRHR1
|Chromosome=17
|position=45733894
|Orientation=plus
|GMAF=0.4679
|Gene_s=CRHR1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 28.3 | 56.6 | 15.0
| HCB | 24.8 | 56.9 | 18.2
| JPT | 32.7 | 54.0 | 13.3
| YRI | 2.7 | 38.1 | 59.2
| ASW | 3.5 | 31.6 | 64.9
| CHB | 24.8 | 56.9 | 18.2
| CHD | 17.4 | 54.1 | 28.4
| GIH | 18.8 | 47.5 | 33.7
| LWK | 10.9 | 31.8 | 57.3
| MEX | 37.9 | 36.2 | 25.9
| MKK | 8.3 | 50.6 | 41.0
| TSI | 18.6 | 44.1 | 37.3
| HapMapRevision=28
}}{{PMID Auto
|PMID=20951764
|Title=High cerebrospinal tau levels are associated with the rs242557 tau gene variant and low cerebrospinal ?-amyloid in Parkinson disease
}}

{{PMID Auto
|PMID=19022385
|Title=5'-Upstream variants of CRHR1 and MAPT genes associated with age at onset in progressive supranuclear palsy and cortical basal degeneration.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}