{{Rsnum
|rsid=9574565
|Chromosome=13
|position=80094739
|Orientation=plus
|GMAF=0.298
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 61.1 | 29.2 | 9.7
| HCB | 70.8 | 25.5 | 3.6
| JPT | 76.1 | 23.0 | 0.9
| YRI | 11.6 | 44.5 | 43.8
| ASW | 14.0 | 52.6 | 33.3
| CHB | 70.8 | 25.5 | 3.6
| CHD | 84.4 | 13.8 | 1.8
| GIH | 33.7 | 50.5 | 15.8
| LWK | 9.1 | 53.6 | 37.3
| MEX | 67.2 | 27.6 | 5.2
| MKK | 14.1 | 53.8 | 32.1
| TSI | 60.4 | 34.7 | 5.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=20023658
|Trait=Nonsyndromic cleft lip with or without cleft palate
|Title=Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate
|RiskAllele=C
|Pval=3E-7
|OR=1.31
|ORtxt=[1.01-1.70]
}}
Associated with European Facial [[Appearance]] {{doi|10.1371/journal.pgen.1002932}}
*[[rs7590268]]
*[[rs16903544]]
*[[rs987525]]
*[[rs9574565]]
*[[rs227731]]
*[[rs642961]] 
*[[rs1258763]]

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs9574565
|overall_frequency_n=77
|overall_frequency_d=126
|overall_frequency=0.611111
|n_genomes=42
|n_genomes_annotated=0
|n_haplomes=65
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

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