TSPAN9, tetraspanin 9, 10867

N. diseases: 18; N. variants: 15
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: rs632887
rs632887
12 3283185 3 prime UTR variant A/G snv 0.44
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 3 2019 2019
dbSNP: rs10491967
rs10491967
12 3258927 intron variant G/A snv 0.21
Creatinine measurement, serum (procedure)
0.700 1.000 1 2016 2016
dbSNP: rs10491967
rs10491967
12 3258927 intron variant G/A snv 0.21
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2016 2016
dbSNP: rs10848820
rs10848820
12 3187782 intron variant A/G snv 0.97
CUI: C2239219
Disease: von Willebrand's factor (lab test)
von Willebrand's factor (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs10848835
rs10848835
12 3232344 intron variant G/C snv 8.4E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019
dbSNP: rs11062517
rs11062517
12 3126673 intron variant C/A;G;T snv
Platelet Component Distribution Width Measurement
0.700 1.000 1 2016 2016
dbSNP: rs12580347
rs12580347
12 3279766 intron variant T/C snv 0.42
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2019 2019
dbSNP: rs16930370
rs16930370
12 3278531 synonymous variant T/C snv 0.16 0.20
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2019 2019
dbSNP: rs16930370
rs16930370
12 3278531 synonymous variant T/C snv 0.16 0.20
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs2011973
rs2011973
1.000 0.080 12 3224412 intron variant C/G;T snv
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs3782774
rs3782774
1.000 0.040 12 3262065 intron variant A/G snv 0.38
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
Cardiovascular Diseases 0.700 1.000 1 2018 2018
dbSNP: rs3782787
rs3782787
12 3249095 intron variant C/A;G snv
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2018 2018
dbSNP: rs3782787
rs3782787
12 3249095 intron variant C/A;G snv
Creatinine measurement, serum (procedure)
0.700 1.000 1 2018 2018
dbSNP: rs544668
rs544668
12 3278838 intron variant T/C snv 0.40
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.700 1.000 1 2018 2018
dbSNP: rs61916264
rs61916264
12 3109418 intron variant A/G snv 0.12
CUI: C4317009
Disease: Diverticular Diseases
Diverticular Diseases
Digestive System Diseases 0.700 1.000 1 2018 2018
dbSNP: rs67551338
rs67551338
12 3283934 3 prime UTR variant C/T snv 4.2E-02
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.700 1.000 1 2017 2017
dbSNP: rs67551338
rs67551338
12 3283934 3 prime UTR variant C/T snv 4.2E-02
Creatinine measurement, serum (procedure)
0.700 1.000 1 2017 2017
dbSNP: rs7963344
rs7963344
12 3122550 intron variant C/T snv 0.18
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs933414
rs933414
12 3103092 intron variant C/T snv 0.39
CUI: C0042834
Disease: Vital capacity
Vital capacity
0.700 1.000 1 2019 2019