Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs14403
rs14403 		1.000 0.040 1 243500591 3 prime UTR variant C/T snv 0.17
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.800 1.000 3 2013 2019
dbSNP: rs6703335
rs6703335 		0.882 0.040 1 243445665 intron variant A/G snv 0.50
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.800 1.000 2 2011 2013
dbSNP: rs12145833
rs12145833 		1.000 0.080 1 243320452 intron variant T/G snv 0.11
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.800 1.000 1 2010 2010
dbSNP: rs1538774
rs1538774 		1.000 0.040 1 243381525 intron variant C/G snv 0.78
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.800 1.000 1 2013 2013
dbSNP: rs10803138
rs10803138 		1.000 0.040 1 243391917 intron variant A/G snv 0.77
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 3 2017 2019
dbSNP: rs12042959
rs12042959 		1 243369971 intron variant A/G;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs2802729
rs2802729 		1 243338461 intron variant C/A;G;T snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 2 2016 2019
dbSNP: rs397515337
rs397515337 		0.925 1 243305133 missense variant C/T snv 1.2E-04 6.3E-05
CUI: C3889474
Disease: BARDET-BIEDL SYNDROME 16
BARDET-BIEDL SYNDROME 16 		0.700 1.000 2 2010 2011
dbSNP: rs397515337
rs397515337 		0.925 1 243305133 missense variant C/T snv 1.2E-04 6.3E-05
CUI: C3150877
Disease: SENIOR-LOKEN SYNDROME 7
SENIOR-LOKEN SYNDROME 7 		0.700 1.000 2 2010 2011
dbSNP: rs77149735
rs77149735 		1.000 0.040 1 243391803 intron variant G/A snv 2.0E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 2 2014 2015
dbSNP: rs10158537
rs10158537 		1 243324884 intron variant C/G;T snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs10803130
rs10803130 		1 243258102 intron variant A/G snv 0.43
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs10926991
rs10926991 		1 243329265 intron variant A/G snv 0.30
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2019 2019
dbSNP: rs12042959
rs12042959 		1 243369971 intron variant A/G;T snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs12093576
rs12093576 		1 243492595 intron variant C/T snv 0.47
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs12741781
rs12741781 		1 243264850 intron variant T/G snv 0.29
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs12748751
rs12748751 		1 243477579 intron variant A/G snv 0.51
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2256126
rs2256126 		1.000 0.040 1 243340806 intron variant A/G snv 0.27
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2019 2019
dbSNP: rs2256126
rs2256126 		1.000 0.040 1 243340806 intron variant A/G snv 0.27
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs2490391
rs2490391 		1.000 0.080 1 243306367 3 prime UTR variant A/C snv 0.50
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2490391
rs2490391 		1.000 0.080 1 243306367 3 prime UTR variant A/C snv 0.50
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs2490395
rs2490395 		1 243295620 intron variant A/G snv 0.48
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2802729
rs2802729 		1 243338461 intron variant C/A;G;T snv
CUI: C0201976
Disease: Creatinine measurement, serum (procedure)
Creatinine measurement, serum (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs28599724
rs28599724 		1 243267516 intron variant C/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs3006917
rs3006917 		1 243478669 intron variant C/T snv 0.21
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019