Source: ALL

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: rs12489732
rs12489732
NT5DC2
3 52532804 intron variant C/A snv 0.26
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs12489828
rs12489828
NT5DC2
3 52532998 intron variant G/T snv 0.51
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs12489828
rs12489828
NT5DC2
3 52532998 intron variant G/T snv 0.51
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2017 2017
dbSNP: rs12489828
rs12489828
NT5DC2
3 52532998 intron variant G/T snv 0.51
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs12489828
rs12489828
NT5DC2
3 52532998 intron variant G/T snv 0.51
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2017 2017
dbSNP: rs4687625
rs4687625
NT5DC2
3 52529702 intron variant C/T snv 0.37
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs541612392
rs541612392
NT5DC2
1.000 0.040 3 52533952 intron variant A/G snv
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee 		0.700 1.000 1 2018 2018
dbSNP: rs66782572
rs66782572
NT5DC2
3 52533601 missense variant A/G snv 0.48 0.51
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement 		0.700 1.000 1 2016 2016
dbSNP: rs6774097
rs6774097
NT5DC2 ; SMIM4
3 52535464 intron variant C/A snv 0.12
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0.700 1.000 1 2019 2019
dbSNP: rs6774097
rs6774097
NT5DC2 ; SMIM4
3 52535464 intron variant C/A snv 0.12
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.700 1.000 1 2019 2019
dbSNP: rs6778735
rs6778735
NT5DC2
3 52531084 intron variant T/C snv 0.54
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs7614981
rs7614981
NT5DC2
1.000 0.040 3 52532898 intron variant C/A snv 0.51
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs7639267
rs7639267
NT5DC2 ; SMIM4
3 52534789 5 prime UTR variant G/T snv 0.59
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.700 1.000 1 2019 2019