{{Rsnum
|rsid=6063312
|Gene=PREX1
|Chromosome=20
|position=48726522
|Orientation=plus
|GMAF=0.1612
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=PREX1
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 73.5 | 23.0 | 3.5
| HCB | 63.5 | 32.8 | 3.6
| JPT | 57.5 | 30.1 | 12.4
| YRI | 85.7 | 13.6 | 0.7
| ASW | 75.4 | 22.8 | 1.8
| CHB | 63.5 | 32.8 | 3.6
| CHD | 64.2 | 29.4 | 6.4
| GIH | 47.5 | 39.6 | 12.9
| LWK | 80.0 | 20.0 | 0.0
| MEX | 44.8 | 48.3 | 6.9
| MKK | 77.6 | 19.9 | 2.6
| TSI | 73.5 | 25.5 | 1.0
| HapMapRevision=28
}}

{{GWAS Summary
|SNP=rs6063312
|PubMedID=17903302
|Condition=Tonometry
|Gene=PREX1
|Risk Allele=
|pValue=2.00E-006
|OR=NA
|95CI=
|OA=1
}}

{{PharmGKB
|RSID=rs6063312
|Name_s=
|Gene_s=PREX1
|Feature=
|Evidence=PubMed ID:17903302; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness (Initial Sample Size: 644-1,327 individuals, depending on measure (Framingham; Replication Sample Size: NR). This variant is associated with Tonometry.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356426
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6063312
|overall_frequency_n=21
|overall_frequency_d=128
|overall_frequency=0.164062
|n_genomes=13
|n_genomes_annotated=0
|n_haplomes=13
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}