{{Rsnum
|rsid=740363
|Chromosome=10
|position=118575606
|Orientation=minus
|GMAF=0.3223
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 28.3 | 47.8 | 23.9
| HCB | 76.5 | 22.0 | 1.5
| JPT | 82.0 | 17.1 | 0.9
| YRI | 45.2 | 40.4 | 14.4
| ASW | 52.6 | 42.1 | 5.3
| CHB | 76.5 | 22.0 | 1.5
| CHD | 70.6 | 23.9 | 5.5
| GIH | 51.5 | 38.6 | 9.9
| LWK | 59.3 | 39.8 | 0.9
| MEX | 24.6 | 54.4 | 21.1
| MKK | 43.5 | 44.2 | 12.3
| TSI | 32.4 | 48.0 | 19.6
| HapMapRevision=28
}}

{{GWAS Summary
|SNP=rs740363
|PubMedID=17903304
|Condition=Heart failure
|Gene=KIAA1598
|Risk Allele=
|pValue=9.00E-006
|OR=NA
|95CI=
|OA=1
}}

{{PharmGKB
|RSID=rs740363
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:17903304; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes (Initial Sample Size: 1,341-1,345 individuals, depending on measure (Framingham; Replication Sample Size: NR). This variant is associated with Heart failure.
|Drugs=
|Drug Classes=
|Diseases=Heart Failure
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356432
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs740363
|overall_frequency_n=44
|overall_frequency_d=128
|overall_frequency=0.34375
|n_genomes=32
|n_genomes_annotated=0
|n_haplomes=41
|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 | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}