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: rs9357271
rs9357271
BTBD9
0.776 0.160 6 38398097 intron variant T/C snv 0.38
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.880 1.000 1 2007 2019
dbSNP: rs3923809
rs3923809
BTBD9
1.000 0.080 6 38473194 intron variant A/G snv 0.32
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.820 1.000 1 2007 2017
dbSNP: rs9296249
rs9296249
BTBD9
0.882 0.120 6 38398065 intron variant T/C snv 0.30
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.820 1.000 1 2007 2017
dbSNP: rs10947723
rs10947723
BTBD9
1.000 0.040 6 38254242 intron variant A/G snv 0.46
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1118268
rs1118268
BTBD9 ; LOC105375045
1.000 0.040 6 38245315 intron variant G/C snv 0.58
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs114407411
rs114407411
BTBD9
1.000 0.040 6 38383336 intron variant G/A snv 6.0E-03
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs114407411
rs114407411
BTBD9
1.000 0.040 6 38383336 intron variant G/A snv 6.0E-03
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2015 2015
dbSNP: rs12191476
rs12191476
BTBD9
1.000 0.040 6 38255610 intron variant C/T snv 0.37
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs12194178
rs12194178
BTBD9 ; LOC105375045
1.000 0.040 6 38243021 intron variant T/C snv 0.37
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs13194038
rs13194038
BTBD9
1.000 0.040 6 38262453 intron variant A/G;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs150713181
rs150713181
BTBD9
1.000 0.040 6 38371756 intron variant T/G snv 6.1E-03
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2015 2015
dbSNP: rs150713181
rs150713181
BTBD9
1.000 0.040 6 38371756 intron variant T/G snv 6.1E-03
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs16890436
rs16890436
BTBD9
1.000 0.040 6 38208938 intron variant G/A snv 4.6E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs16890509
rs16890509
BTBD9
1.000 0.040 6 38247425 intron variant T/C;G snv 7.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs16890511
rs16890511
BTBD9
1.000 0.040 6 38247828 intron variant T/C snv 3.2E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs16890522
rs16890522
BTBD9
1.000 0.040 6 38268526 intron variant G/A;C;T snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs16890541
rs16890541
BTBD9
1.000 0.040 6 38279615 intron variant C/G snv 0.12
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs17757975
rs17757975
BTBD9 ; LOC105375045
6 38246374 intron variant T/C snv 0.12
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs192452148
rs192452148
BTBD9
1.000 0.040 6 38387529 intron variant C/T snv 6.0E-03
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.700 1.000 1 2015 2015
dbSNP: rs192452148
rs192452148
BTBD9
1.000 0.040 6 38387529 intron variant C/T snv 6.0E-03
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs1931760
rs1931760
BTBD9
1.000 0.040 6 38233669 intron variant C/A snv 0.11
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs4299828
rs4299828
BTBD9
1.000 0.040 6 38209891 intron variant G/A;C snv
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs4711527
rs4711527
BTBD9 ; LOC105375045
1.000 0.040 6 38241833 intron variant C/T snv 0.83
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs4714131
rs4714131
BTBD9
1.000 0.040 6 38221260 intron variant T/C snv 0.80
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs4714135
rs4714135
BTBD9
1.000 0.040 6 38248618 intron variant G/A snv 2.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017