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: rs4141463
rs4141463
MACROD2
0.925 0.040 20 14766825 intron variant T/C snv 0.50
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		0.820 0.667 1 2010 2019
dbSNP: rs6110278
rs6110278
MACROD2
20 14407569 intron variant C/T snv 0.27
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.800 1.000 1 2009 2009
dbSNP: rs1041606
rs1041606
MACROD2
20 14697142 intron variant C/T snv 0.21
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate 		0.700 1.000 1 2019 2019
dbSNP: rs10485775
rs10485775
MACROD2
1.000 0.040 20 14707123 intron variant T/G snv 0.21
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11087114
rs11087114
MACROD2 ; MACROD2-AS1
20 14931037 intron variant G/A;C snv
CUI: C0019693
Disease: HIV Infections
HIV Infections 		0.700 1.000 1 2017 2017
dbSNP: rs11907538
rs11907538
MACROD2
1.000 0.040 20 14709539 intron variant C/T snv 7.5E-02
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs11908097
rs11908097
MACROD2
20 14708500 intron variant T/C snv 0.17
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs11908351
rs11908351
MACROD2
1.000 0.040 20 14705863 intron variant A/T snv 0.20
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs13038351
rs13038351
MACROD2
20 14486741 intron variant A/T snv 0.16
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs16996644
rs16996644
MACROD2
20 15832830 intron variant C/G snv 0.13
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs16996657
rs16996657
MACROD2
20 15835591 intron variant T/C snv 0.16
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs175804
rs175804
MACROD2
20 15851654 intron variant A/C;T snv
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2015 2015
dbSNP: rs17775664
rs17775664
MACROD2
1.000 0.040 20 14707873 intron variant G/T snv 0.30
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs1932952
rs1932952
MACROD2
20 14701155 intron variant G/C snv 0.37
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2423958
rs2423958
MACROD2
20 15365019 intron variant C/A snv 0.49
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs401599
rs401599
MACROD2
20 14830831 intron variant A/C snv 0.44
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs465757
rs465757
MACROD2
20 15599638 intron variant G/A snv 0.60
CUI: C2697758
Disease: Interleukin 10 Measurement
Interleukin 10 Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs6034019
rs6034019
MACROD2
20 14722269 intron variant A/G snv 0.68
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs6034146
rs6034146
MACROD2
20 15293250 intron variant A/C snv 0.60
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs6042935
rs6042935
MACROD2
20 14816926 intron variant A/G snv 8.2E-02
CUI: C0201534
Disease: Antiphospholipid antibodies measurement
Antiphospholipid antibodies measurement 		0.700 1.000 1 2016 2016
dbSNP: rs6043189
rs6043189
MACROD2
1.000 0.040 20 15300687 intron variant A/G snv 0.47
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs6043194
rs6043194
MACROD2
1.000 0.040 20 15301802 intron variant G/A snv 0.23
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.700 1.000 1 2017 2017
dbSNP: rs6043200
rs6043200
MACROD2
20 15314273 intron variant G/A snv 0.33
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs6074798
rs6074798
MACROD2
20 14781064 intron variant G/A snv 0.40
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs6079463
rs6079463
MACROD2
1.000 0.040 20 14495111 intron variant A/G snv 0.26
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder 		0.700 1.000 1 2019 2019