{{Genotype
|rsid=1711437
|allele1=G
|allele2=G
|magnitude=2.4
|repute=Bad
|summary=slightly reduced creatinine clearance
}}
In the BLSA population, the genotype of rs1711437 explains 2.1% of the variation in creatinine clearance and in the InCHIANTI population, the genotype explains 0.9% of the variation.  G is the risk allele.  For an individual who carries two copies of the G allele, his or her creatinine clearance is approximately that of someone 4–5 years younger who carries 0 or 1 allele (A;A or A;G).

The association between rs1711437 genotype and creatinine clearance has not been replicated in additional populations.