{{Rsnum
|rsid=6108011
|Chromosome=20
|position=7571857
|Orientation=plus
|GMAF=0.2594
|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 | 49.6 | 38.1 | 12.4
| HCB | 50.4 | 40.9 | 8.8
| JPT | 65.5 | 27.4 | 7.1
| YRI | 61.9 | 32.0 | 6.1
| ASW | 68.4 | 28.1 | 3.5
| CHB | 50.4 | 40.9 | 8.8
| CHD | 55.0 | 40.4 | 4.6
| GIH | 63.4 | 29.7 | 6.9
| LWK | 61.8 | 34.5 | 3.6
| MEX | 60.3 | 32.8 | 6.9
| MKK | 53.2 | 39.7 | 7.1
| TSI | 56.9 | 35.3 | 7.8
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=17903294
|Trait=Hemostatic factors and hematological phenotypes
|Title=Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study
|RiskAllele=
|Pval=0.0000060000000000000002
|OR=NR
|ORtxt=NR
|OA=1
}}

{{PMID Auto
|PMID=17186469
|Title=Mutations in the gene encoding the Wnt-signaling component R-spondin 4 (RSPO4) cause autosomal recessive anonychia.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6108011
|overall_frequency_n=26
|overall_frequency_d=128
|overall_frequency=0.203125
|n_genomes=17
|n_genomes_annotated=0
|n_haplomes=21
|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 | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}