{{Rsnum
|rsid=7203560
|Gene=NPRL3
|Chromosome=16
|position=134391
|Orientation=plus
|GMAF=0.01928
|Gene_s=NPRL3
|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 | 0.0 | 0.0 | 100.0
| HCB | 0.0 | 0.0 | 100.0
| JPT | 0.0 | 0.0 | 100.0
| YRI | 1.4 | 23.9 | 74.6
| ASW | 0.0 | 14.3 | 85.7
| CHB | 0.0 | 0.0 | 100.0
| CHD | 0.9 | 0.0 | 99.1
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 5.5 | 94.5
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 7.1 | 92.9
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23263863
  |Trait=Hematology traits
  |Title=GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
  |RiskAllele=G
  |Pval=2E-8
  |OR=.20
  |ORtxt=[0.13-0.27] unit decrease
  |OA=1
}}

{{PMID Auto GWAS
  |PMID=23406172
  |Trait=Sickle cell anemia (haemolysis)
  |Title=Genetic determinants of haemolysis in sickle cell anaemia.
  |RiskAllele=C
  |Pval=2E-9
  |OR=.44
  |ORtxt=[0.30-0.58] unit decrease
  }}

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