{{Rsnum
|rsid=2990510
|Gene=F13B
|Chromosome=1
|position=197051528
|Orientation=plus
|GMAF=0.2397
|Gene_s=F13B
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 11.5 | 54.0 | 34.5
| HCB | 1.5 | 25.5 | 73.0
| JPT | 1.8 | 26.5 | 71.7
| YRI | 0.7 | 23.1 | 76.2
| ASW | 7.0 | 24.6 | 68.4
| CHB | 1.5 | 25.5 | 73.0
| CHD | 0.9 | 16.5 | 82.6
| GIH | 6.9 | 34.7 | 58.4
| LWK | 2.7 | 20.0 | 77.3
| MEX | 10.5 | 36.8 | 52.6
| MKK | 2.6 | 28.2 | 69.2
| TSI | 15.0 | 39.0 | 46.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=22704111
|Trait=None
|Title=Pilot Genome-Wide Association Search Identifies Potential Loci for Risk of Erectile Dysfunction in Type 1 Diabetes Using the DCCT/EDIC Study Cohort.
|RiskAllele=G
|Pval=0.000006
|OR=None
|ORtxt=None
|OA=1
}}

{{PMID Auto
|PMID=18541031
|Title=The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration.
|OA=1
}}

{{on chip | Illumina Human 1M}}