MEF2C-AS1, MEF2C antisense RNA 1, 101929423

N. diseases: 23; N. variants: 36
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1366594
rs1366594 		5 89080244 intron variant A/C snv 0.57
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 3 2009 2018
dbSNP: rs190982
rs190982 		0.925 0.080 5 88927603 intron variant G/A snv 0.72
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.800 1.000 1 2013 2013
dbSNP: rs62378245
rs62378245 		1.000 0.040 5 89448145 intron variant C/T snv 0.25
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 4 2015 2019
dbSNP: rs1366594
rs1366594 		5 89080244 intron variant A/C snv 0.57
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		0.700 1.000 3 2011 2014
dbSNP: rs16867576
rs16867576 		1.000 0.040 5 89450514 intron variant A/G snv 0.18
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 3 2014 2019
dbSNP: rs10037512
rs10037512 		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 		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: rs2067663
rs2067663 		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: rs770463
rs770463 		5 88899133 intron variant C/T snv 0.61
CUI: C0021704
Disease: Intelligence
Intelligence 		Behavior and Behavior Mechanisms 0.700 1.000 2 2018 2018
dbSNP: rs10037512
rs10037512 		5 89058858 intron variant T/A;C snv
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010
dbSNP: rs10037512
rs10037512 		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 		5 88894787 intron variant A/T snv 0.52
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs114694170
rs114694170 		1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs114694170
rs114694170 		1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02
CUI: C2239222
Disease: Vascular Endothelial Growth Factor Measurement
Vascular Endothelial Growth Factor Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs114694170
rs114694170 		1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02
CUI: C3828530
Disease: Platelet Component Distribution Width Measurement
Platelet Component Distribution Width Measurement 		0.700 1.000 1 2016 2016
dbSNP: rs114694170
rs114694170 		1.000 0.040 5 88884379 non coding transcript exon variant T/C snv 3.6E-02
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs12522630
rs12522630 		5 88892550 intron variant G/A snv 4.2E-02
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		0.700 1.000 1 2013 2013
dbSNP: rs13170203
rs13170203 		5 89317824 intron variant T/A;C snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1366594
rs1366594 		5 89080244 intron variant A/C snv 0.57
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs141568462
rs141568462 		1.000 0.080 5 89179048 intron variant T/C snv 5.5E-04
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2016 2016
dbSNP: rs17494872
rs17494872 		5 88897342 intron variant G/A snv 4.2E-02
CUI: C0177804
Disease: Bone Mineral Density Test
Bone Mineral Density Test 		0.700 1.000 1 2013 2013
dbSNP: rs17499351
rs17499351 		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 		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 		5 88887834 intron variant A/G snv 0.18
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2014 2014
dbSNP: rs186292051
rs186292051 		1.000 0.080 5 89030013 intron variant C/T snv 4.0E-03
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2016 2016