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: rs1531070
rs1531070
MAML3
0.851 0.120 4 139874173 intron variant G/A snv 0.30
CUI: C0158611
Disease: Other congenital anomalies of heart
Other congenital anomalies of heart 		0.800 1.000 1 2013 2013
dbSNP: rs1531070
rs1531070
MAML3
0.851 0.120 4 139874173 intron variant G/A snv 0.30
CUI: C0018798
Disease: Congenital Heart Defects
Congenital Heart Defects 		0.800 1.000 1 2013 2013
dbSNP: rs1531070
rs1531070
MAML3
0.851 0.120 4 139874173 intron variant G/A snv 0.30
CUI: C0478009
Disease: Congenital malformation of cardiac chambers and connections, unspecified
Congenital malformation of cardiac chambers and connections, unspecified 		0.800 1.000 1 2013 2013
dbSNP: rs1531070
rs1531070
MAML3
0.851 0.120 4 139874173 intron variant G/A snv 0.30
CUI: C3554279
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2 		0.800 1.000 1 2013 2013
dbSNP: rs1531070
rs1531070
MAML3
0.851 0.120 4 139874173 intron variant G/A snv 0.30
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		0.800 1.000 1 2013 2013
dbSNP: rs1531070
rs1531070
MAML3
0.851 0.120 4 139874173 intron variant G/A snv 0.30
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		0.800 1.000 1 2013 2013
dbSNP: rs57800857
rs57800857
MAML3
4 139942211 intron variant A/C;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2019 2019
dbSNP: rs10030552
rs10030552
MAML3
4 140051110 intron variant C/A snv 0.24
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs11100307
rs11100307
MAML3
1.000 0.040 4 139846549 intron variant T/C snv 0.28
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2019 2019
dbSNP: rs11100307
rs11100307
MAML3
1.000 0.040 4 139846549 intron variant T/C snv 0.28
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs12643771
rs12643771
MAML3
4 139831949 intron variant C/T snv 0.25
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs17373738
rs17373738
MAML3
4 140014110 intron variant C/G snv 0.26
CUI: C0037369
Disease: Smoking
Smoking 		0.700 1.000 1 2019 2019
dbSNP: rs1869717
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure 		0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14
CUI: C0018801
Disease: Heart failure
Heart failure 		0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		0.700 1.000 1 2016 2016
dbSNP: rs1869717
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		0.700 1.000 1 2016 2016