Source: GWASCAT

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: rs73962318
rs73962318
ARHGAP15 ; MTND4P22
2 143097365 non coding transcript exon variant T/C snv 4.2E-02
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2015 2015
dbSNP: rs73962318
rs73962318
ARHGAP15 ; MTND4P22
2 143097365 non coding transcript exon variant T/C snv 4.2E-02
CUI: C1519383
Disease: Smoking Behaviors
Smoking Behaviors 		0.700 1.000 1 2015 2015
dbSNP: rs140397066
rs140397066
ARHGAP15
2 143404536 intron variant A/G snv 3.1E-03
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs35125029
rs35125029
ARHGAP15
2 143504088 intron variant G/A snv 0.26
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		0.700 1.000 1 2016 2016
dbSNP: rs74847330
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs74847330
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs79716587
rs79716587
ARHGAP15
2 143129250 intron variant G/A snv 7.9E-02
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2016 2016
dbSNP: rs79716587
rs79716587
ARHGAP15
2 143129250 intron variant G/A snv 7.9E-02
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs10191758
rs10191758
ARHGAP15
2 143505711 intron variant A/G snv 0.30
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 2 2017 2017
dbSNP: rs4662344
rs4662344
ARHGAP15
0.925 0.080 2 143591289 intron variant T/C snv 0.82
CUI: C0012813
Disease: Diverticulitis
Diverticulitis 		0.710 1.000 1 2017 2017
dbSNP: rs4662344
rs4662344
ARHGAP15
0.925 0.080 2 143591289 intron variant T/C snv 0.82
CUI: C4317009
Disease: Diverticular Diseases
Diverticular Diseases 		0.710 1.000 1 2017 2017
dbSNP: rs74847330
rs74847330
ARHGAP15
2 143074030 intergenic variant A/G snv 8.8E-02
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2017 2017
dbSNP: rs13428598
rs13428598
ARHGAP15
2 143492918 intron variant C/T snv 0.28
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 3 2018 2019
dbSNP: rs6710871
rs6710871
ARHGAP15
2 143203024 intron variant G/A snv 0.17
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2018 2019
dbSNP: rs6734367
rs6734367
ARHGAP15
2 143556678 intron variant T/A;G snv
CUI: C4317009
Disease: Diverticular Diseases
Diverticular Diseases 		0.700 1.000 2 2018 2019
dbSNP: rs10189912
rs10189912
ARHGAP15
2 143405040 intron variant A/G snv 0.27
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs10204230
rs10204230
ARHGAP15
2 143512879 intron variant T/C snv 0.42
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs12991555
rs12991555
ARHGAP15
2 143429947 intron variant A/G;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs13010737
rs13010737
ARHGAP15
1.000 0.040 2 143442474 intron variant G/A snv 0.36
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2018 2018
dbSNP: rs13413953
rs13413953
ARHGAP15
1.000 0.040 2 143479467 intron variant T/G snv 0.25
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs13413953
rs13413953
ARHGAP15
1.000 0.040 2 143479467 intron variant T/G snv 0.25
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs13428598
rs13428598
ARHGAP15
2 143492918 intron variant C/T snv 0.28
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs2034604
rs2034604
ARHGAP15
0.776 0.160 2 143201176 intron variant C/G;T snv
CUI: C3489529
Disease: Tooth Agenesis, Familial
Tooth Agenesis, Familial 		0.700 1.000 1 2018 2018
dbSNP: rs2034604
rs2034604
ARHGAP15
0.776 0.160 2 143201176 intron variant C/G;T snv
CUI: C1970117
Disease: Tooth Agenesis, Selective, With Orofacial Cleft
Tooth Agenesis, Selective, With Orofacial Cleft 		0.700 1.000 1 2018 2018
dbSNP: rs2034604
rs2034604
ARHGAP15
0.776 0.160 2 143201176 intron variant C/G;T snv
CUI: C1970118
Disease: Hypodontia Oligodontia with Orofacial Cleft
Hypodontia Oligodontia with Orofacial Cleft 		0.700 1.000 1 2018 2018