{{Rsnum
|rsid=4979078
|Gene=SUSD1
|Chromosome=9
|position=112060841
|Orientation=plus
|GMAF=0.2893
|Gene_s=SUSD1
|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 | 2.7 | 23.9 | 73.5
| HCB | 6.6 | 38.0 | 55.5
| JPT | 4.4 | 36.3 | 59.3
| YRI | 31.3 | 49.7 | 19.0
| ASW | 17.5 | 50.9 | 31.6
| CHB | 6.6 | 38.0 | 55.5
| CHD | 5.5 | 31.2 | 63.3
| GIH | 3.0 | 39.6 | 57.4
| LWK | 40.9 | 44.5 | 14.5
| MEX | 8.6 | 48.3 | 43.1
| MKK | 17.3 | 53.8 | 28.8
| TSI | 2.9 | 18.6 | 78.4
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23650146
  |Trait=Venous thromboembolism
  |Title=A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
  |RiskAllele=C
  |Pval=3E-6
  |OR=1.21
  |ORtxt=[1.11-1.30]
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | FTDNA}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}