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: 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: 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: 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
dbSNP: rs2034604
rs2034604
ARHGAP15
0.776 0.160 2 143201176 intron variant C/G;T snv
CUI: C0020608
Disease: Hypodontia
Hypodontia 		0.700 1.000 1 2018 2018
dbSNP: rs2034604
rs2034604
ARHGAP15
0.776 0.160 2 143201176 intron variant C/G;T snv
CUI: C4082304
Disease: Oligodontia
Oligodontia 		0.700 1.000 1 2018 2018
dbSNP: rs4273169
rs4273169
ARHGAP15
1.000 0.040 2 143473740 intron variant G/A;C snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs4273169
rs4273169
ARHGAP15
1.000 0.040 2 143473740 intron variant G/A;C snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs62171698
rs62171698
ARHGAP15
2 143201527 intron variant C/A;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
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: rs62172064
rs62172064
ARHGAP15
2 143397319 intron variant T/C snv 1.2E-02
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
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: 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: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
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: 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: 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: 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