{{Rsnum
|rsid=10883969
|Gene=SFR1
|Chromosome=10
|position=105884116
|Orientation=plus
|GMAF=0.3356
|Gene_s=SFR1
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 31.0 | 43.4 | 25.7
| HCB | 30.7 | 54.0 | 15.3
| JPT | 24.8 | 54.0 | 21.2
| YRI | 0.0 | 0.0 | 0.0
| ASW | 78.9 | 21.1 | 0.0
| CHB | 30.7 | 54.0 | 15.3
| CHD | 34.9 | 52.3 | 12.8
| GIH | 48.5 | 41.6 | 9.9
| LWK | 0.0 | 0.0 | 0.0
| MEX | 41.4 | 51.7 | 6.9
| MKK | 79.5 | 19.9 | 0.6
| TSI | 30.4 | 50.0 | 19.6
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23551011
  |Trait=Preeclampsia
  |Title=Genome-Wide Association Study of Pre-Eclampsia Detects Novel Maternal Single Nucleotide Polymorphisms and Copy-Number Variants in Subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) Study Cohort.
  |RiskAllele=
  |Pval=3E-6
  |OR=2.97
  |ORtxt=[1.88-4.69]
  }}

{{on chip | FTDNA}}
{{on chip | Illumina Human 1M}}