RS10887800 RNLS

Health Risk Chr 10:88316085 snv intron variant

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What This Variant Does

"Polymorphism of the renalase gene in end-stage renal disease patients affected by hypertension"

Associated Conditions

Family history

Population Frequencies

1kG AFR

29.2%

1kG ALL

53.2%

1kG AMR

54.9%

1kG EAS

51.4%

1kG EUR

51.7%

1kG SAS

61.9%

Other Variants in RNLS