rs12917707

Parent Gene: PDILT, UMOD

Importance: 5
Less common allele: T = 10%
More common allele: G = 90%
My Genotype: Log In
Risk Allele: G, T, T, T, T, T, T, T, T, T

Disease/Trait: Chronic Kidney Disease

The G allele of rs12917707 is reported to be associated with Chronic Kidney Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Renal function and chronic kidney disease (CKD).

Disease/Trait: Renal System Measurement

The T allele of rs12917707 is reported to be associated with Renal System Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Renal function and chronic kidney disease (eGFRcrea).

Disease/Trait: Urinary Uromodulin Measurement

The T allele of rs12917707 is reported to be associated with Urinary Uromodulin Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Urinary uromodulin levels.

Disease/Trait: Gfr Change Measurement

The T allele of rs12917707 is reported to be associated with Gfr Change Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Kidney function decline traits (eGFRchange overall).

Disease/Trait: Gfr Change Measurement

The T allele of rs12917707 is reported to be associated with Gfr Change Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Kidney function decline traits (eGFRchange noCKD).

Disease/Trait: Chronic Kidney Disease

The T allele of rs12917707 is reported to be associated with Chronic Kidney Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Kidney function decline traits (CKDi).

Disease/Trait: Chronic Kidney Disease

The T allele of rs12917707 is reported to be associated with Chronic Kidney Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Kidney function decline traits (CKDi25).

Disease/Trait: Diabetes Mellitus

The T allele of rs12917707 is reported to be associated with Diabetes Mellitus (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Glomerular filtration rate in diabetics (creatinine).

Disease/Trait: Serum Creatinine Measurement

The T allele of rs12917707 is reported to be associated with Serum Creatinine Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Glomerular filtration rate in diabetics (creatinine).

Disease/Trait: Glomerular Filtration Rate

The T allele of rs12917707 is reported to be associated with Glomerular Filtration Rate (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Glomerular filtration rate in diabetics (creatinine).

Disease/Trait: Chronic Kidney Disease

The T allele of rs12917707 is reported to be associated with Chronic Kidney Disease (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Chronic kidney disease (eGFRcrea).

Disease/Trait: Serum Creatinine Measurement

The T allele of rs12917707 is reported to be associated with Serum Creatinine Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Chronic kidney disease (eGFRcrea).

Disease/Trait: Serum Creatinine Measurement

The T allele of rs12917707 is reported to be associated with Serum Creatinine Measurement (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Glomerular filtration rate in non diabetics (creatinine).

Disease/Trait: Glomerular Filtration Rate

The T allele of rs12917707 is reported to be associated with Glomerular Filtration Rate (R) . Your genotype was not identified for this SNP so we are unable to comment on your association with Glomerular filtration rate in non diabetics (creatinine).