{{Rsnum
|rsid=1378942
|Gene=CSK
|Chromosome=15
|position=74785026
|Orientation=minus
|GMAF=0.3301
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene_s=CSK
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 12.5 | 39.3 | 48.2
| HCB | 62.0 | 33.6 | 4.4
| JPT | 63.7 | 31.0 | 5.3
| YRI | 100.0 | 0.0 | 0.0
| ASW | 75.4 | 24.6 | 0.0
| CHB | 62.0 | 33.6 | 4.4
| CHD | 75.9 | 23.1 | 0.9
| GIH | 76.2 | 21.8 | 2.0
| LWK | 95.5 | 4.5 | 0.0
| MEX | 48.3 | 39.7 | 12.1
| MKK | 59.0 | 32.7 | 8.3
| TSI | 24.5 | 45.1 | 30.4
| HapMapRevision=28
}}

[http://blog.23andme.com/2009/05/12/snpwatch-researchers-find-more-genetic-variations-associated-with-blood-pressure/ 23andMe blog] [[blood pressure]]

{{PMID Auto GWAS
|PMID=19430483
|Trait=Diastolic Blood Pressure
|Title=Genome-wide association study identifies eight loci associated with blood pressure
|RiskAllele=C
|Pval=1E-23
|OR=0.43
|ORtxt=[0.35-0.51] mm Hg increase
|OA=1
}}

{{PMID Auto
|PMID=19960030
|Title=Genetic variations in ATP2B1, CSK, ARSG and CSMD1 loci are related to blood pressure and/or hypertension in two Korean cohorts
}}

{{PMID Auto
|PMID=20921432
|Title=Common Variants in the ATP2B1 Gene Are Associated With Susceptibility to Hypertension. The Japanese Millennium Genome Project
}}

{{PMID Auto GWAS
|PMID=21909115
|Trait=None
|Title=Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk.
|RiskAllele=C
|Pval=3E-26
|OR=0.4160
|ORtxt=[NR] mmHg increase
|OA=1
}}

{{PMID Auto GWAS
|PMID=21909110
|Trait=None
|Title=Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.
|RiskAllele=C
|Pval=2E-15
|OR=0.3860
|ORtxt=[0.29-0.48] mmHg increase
|OA=1
}}

{{PMID Auto
|PMID=22492992
|Title=Caffeine intake and CYP1A2 variants associated with high caffeine intake protect non-smokers from hypertension.
}}

{{PMID Auto
|PMID=22525200
|Title=Pharmacogenetic implications for eight common blood pressure-associated single-nucleotide polymorphisms.
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1378942
|overall_frequency_n=39
|overall_frequency_d=128
|overall_frequency=0.304688
|n_genomes=24
|n_genomes_annotated=0
|n_haplomes=34
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

[[High Blood Pressure (Hypertension)]]

{{PMID Auto
|PMID=23946333
|Title=Identification of the PTPN22 functional variant R620W as susceptibility genetic factor for giant cell arteritis
}}

{{PMID Auto
|PMID=24401815
|Title=Interaction between c-Src Tyrosine Kinase Gene Variant and Fish Oil Intake Influences Blood Pressure in Healthy Adults
}}

{{PMID Auto
|PMID=22959498
|Title=Recapitulation of four hypertension susceptibility genes (CSK, CYP17A1, MTHFR, and FGF5) in East Asians.
}}

{{PMID Auto
|PMID=23102448
|Title=Physical activity modifies the associations between genetic variants and hypertension in the Chinese children.
}}

{{PMID Auto
|PMID=23591986
|Title=Influence of obesity on association between genetic variants identified by genome-wide association studies and hypertension risk in Chinese children.
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}