{{Rsnum
|rsid=2968864
|Chromosome=7
|position=150925074
|Orientation=minus
|GMAF=0.1313
|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 | 55.8 | 38.1 | 6.2
| HCB | 92.7 | 6.6 | 0.7
| JPT | 92.9 | 7.1 | 0.0
| YRI | 100.0 | 0.0 | 0.0
| ASW | 89.5 | 10.5 | 0.0
| CHB | 92.7 | 6.6 | 0.7
| CHD | 89.0 | 9.2 | 1.8
| GIH | 59.4 | 32.7 | 7.9
| LWK | 98.2 | 1.8 | 0.0
| MEX | 72.4 | 25.9 | 1.7
| MKK | 94.2 | 5.8 | 0.0
| TSI | 50.0 | 41.2 | 8.8
| HapMapRevision=28
}}
[http://blog.23andme.com/2009/03/23/snpwatch-researchers-identify-genetic-variants-linked-to-heart-rhythm-and-possibly-sudden-cardiac-death/ 23andMe blog] Influences [[QT interval]]

{{PMID Auto GWAS
|PMID=19305408
|Trait=QT interval
|Title=Common variants at ten loci influence QT interval duation in the QTGEN Study
|RiskAllele=C
|Pval=8E-16
|OR=1.40
|ORtxt=[1.06-1.74] msec decrease
|OA=1
}}

{{PharmGKB
|RSID=rs2968864
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:19305408; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Common variants at ten loci influence QT interval duation in the QTGEN Study. (Initial Sample Size: 13,685 individuals; Replication Sample Size: 15,854 individuals); (Region: 7q36.1; Reported Gene(s): KCNH2; Risk Allele: rs2968864-C); (p-value= 0.0000000000000008).This variant is associated with QT interval.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164739895
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2968864
|overall_frequency_n=17
|overall_frequency_d=128
|overall_frequency=0.132812
|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 v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}