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: rs34367533
rs34367533
MEF2C-AS1
5 89188503 intron variant T/C;G snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs34957094
rs34957094
MEF2C-AS1
5 88979517 intron variant -/C ins 2.0E-05
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2017 2017
dbSNP: rs3850651
rs3850651
MEF2C ; MEF2C-AS1
5 88885292 intron variant T/A;C;G snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs4916737
rs4916737
MEF2C-AS1
5 88994950 intron variant G/T snv 0.44
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4916751
rs4916751
MEF2C-AS1
5 89453065 intron variant T/G snv 0.69
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs59844455
rs59844455
MEF2C-AS1
5 89003450 intron variant G/A;T snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs62378245
rs62378245
MEF2C-AS1
1.000 0.040 5 89448145 intron variant C/T snv 0.25
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs62378245
rs62378245
MEF2C-AS1
1.000 0.040 5 89448145 intron variant C/T snv 0.25
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2019 2019
dbSNP: rs6892330
rs6892330
MEF2C-AS1
5 89450588 intron variant T/C snv 0.68
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs6894139
rs6894139
MEF2C-AS1
5 89031965 non coding transcript exon variant T/G snv 0.57
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2014 2014
dbSNP: rs6894139
rs6894139
MEF2C-AS1
5 89031965 non coding transcript exon variant T/G snv 0.57
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2014 2014
dbSNP: rs73772144
rs73772144
MEF2C-AS1
5 89305735 intron variant G/A snv 6.5E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs76994193
rs76994193
MEF2C-AS1
1.000 0.040 5 89131520 intron variant A/C;G snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2017 2017
dbSNP: rs76994193
rs76994193
MEF2C-AS1
1.000 0.040 5 89131520 intron variant A/C;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.700 1.000 1 2017 2017
dbSNP: rs7725337
rs7725337
MEF2C-AS1
5 89095690 intron variant T/C snv 0.43
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs7728694
rs7728694
MEF2C-AS1
5 88992524 intron variant G/A;T snv 0.58
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs9293513
rs9293513
MEF2C-AS1
1.000 0.080 5 89337967 intron variant G/A snv 3.0E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2016 2016