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: rs1366594
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 3 2009 2018
dbSNP: rs10037512
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 2 2010 2015
dbSNP: rs2067663
rs2067663
MEF2C ; MEF2C-AS1
5 88895818 intron variant C/T snv 0.22
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 2 2016 2019
dbSNP: rs2067663
rs2067663
MEF2C ; MEF2C-AS1
5 88895818 intron variant C/T snv 0.22
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 2 2016 2019
dbSNP: rs770463
rs770463
MEF2C ; MEF2C-AS1
5 88899133 intron variant C/T snv 0.61
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 2 2018 2018
dbSNP: rs10037512
rs10037512
MEF2C-AS1
5 89058858 intron variant T/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2018 2018
dbSNP: rs10066711
rs10066711
MEF2C ; MEF2C-AS1
5 88894787 intron variant A/T snv 0.52
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1366594
rs1366594
MEF2C-AS1
5 89080244 intron variant A/C snv 0.57
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs17499351
rs17499351
MEF2C-AS1
5 89174513 intron variant T/C snv 3.4E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs17508332
rs17508332
MEF2C-AS1 ; LOC105379074
5 89392546 intron variant C/T snv 3.7E-02
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs17560407
rs17560407
MEF2C ; MEF2C-AS1
5 88887834 intron variant A/G snv 0.18
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2014 2014
dbSNP: rs200572016
rs200572016
MEF2C-AS1
5 88924623 intron variant AG/- delins 2.8E-03
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2067663
rs2067663
MEF2C ; MEF2C-AS1
5 88895818 intron variant C/T snv 0.22
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		0.700 1.000 1 2016 2016
dbSNP: rs2217257
rs2217257
MEF2C-AS1
5 89046775 intron variant C/T snv 0.39
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs304132
rs304132
MEF2C-AS1 ; LOC107986360
5 88919777 intron variant A/G snv 0.67
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs3087054
rs3087054
MEF2C-AS1
5 89439520 intron variant GTGTGTGTGTGT/-;GT;GTGT;GTGTGT;GTGTGTGT;GTGTGTGTGT;GTGTGTGTGTGTGT;GTGTGTGTGTGTGTGT;GTGTGTGTGTGTGTGTGT delins
CUI: C0424621
Disease: Body Fat Distribution
Body Fat Distribution 		0.700 1.000 1 2019 2019
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: 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