Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs138551969
rs138551969
1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2018 2018
dbSNP: rs138551969
rs138551969
1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia
0.700 1.000 1 2018 2018
dbSNP: rs138551969
rs138551969
1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05
Creatinine measurement, serum (procedure)
0.700 1.000 1 2018 2018
dbSNP: rs138551969
rs138551969
1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure)
0.700 1.000 1 2018 2018
dbSNP: rs3025021
rs3025021
0.882 0.160 6 43781426 non coding transcript exon variant T/C snv 0.70
CUI: C2697758
Disease: Interleukin 10 Measurement
Interleukin 10 Measurement
0.700 1.000 1 2017 2017
dbSNP: rs833070
rs833070
0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2016 2016
dbSNP: rs833070
rs833070
0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs833070
rs833070
0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
0.700 1.000 1 2016 2016
dbSNP: rs2010963
rs2010963
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 1(finding)
0.700 0