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: 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: 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: 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: 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: rs10200533
rs10200533
ARHGAP15
2 143425433 intron variant G/A snv 0.54
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
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: rs12465778
rs12465778
ARHGAP15
2 143497632 intron variant T/C snv 0.46
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
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: rs13002158
rs13002158
ARHGAP15
2 143264143 intron variant A/G snv 0.22
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
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: 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: rs141234028
rs141234028
ARHGAP15
2 143570965 intron variant C/T snv 7.7E-03
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs16858573
rs16858573
ARHGAP15
1.000 0.040 2 143118156 intron variant T/C snv 8.7E-02
CUI: C0013595
Disease: Eczema
Eczema 		0.700 1.000 1 2019 2019
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
dbSNP: rs2034604
rs2034604
ARHGAP15
0.776 0.160 2 143201176 intron variant C/G;T snv
CUI: C4310638
Disease: TOOTH AGENESIS, SELECTIVE, 9
TOOTH AGENESIS, SELECTIVE, 9 		0.700 1.000 1 2018 2018
dbSNP: rs2034604
rs2034604
ARHGAP15
0.776 0.160 2 143201176 intron variant C/G;T snv
CUI: C0399352
Disease: Developmental absence of tooth
Developmental absence of tooth 		0.700 1.000 1 2018 2018
dbSNP: rs2034604
rs2034604
ARHGAP15
0.776 0.160 2 143201176 intron variant C/G;T snv
CUI: C0155922
Disease: Tooth development and eruption disorder
Tooth development and eruption disorder 		0.700 1.000 1 2018 2018