MEF2D, myocyte enhancer factor 2D, 4209

N. diseases: 72; N. variants: 10
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: rs2274316
rs2274316 		0.925 0.040 1 156476450 intron variant C/A snv 0.62 0.54
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.820 0.500 4 2012 2017
dbSNP: rs1925950
rs1925950 		1 156480948 missense variant G/A;C snv 0.62
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.800 1.000 2 2012 2016
dbSNP: rs3790455
rs3790455 		1 156486509 intron variant C/T snv 0.54
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.800 1.000 2 2012 2013
dbSNP: rs202206511
rs202206511 		1 156486509 intron variant -/T delins
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.700 1.000 2 2012 2013
dbSNP: rs1050316
rs1050316 		1 156464911 3 prime UTR variant G/T snv 0.54
CUI: C0018681
Disease: Headache
Headache 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2018 2018
dbSNP: rs1050316
rs1050316 		1 156464911 3 prime UTR variant G/T snv 0.54
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1050316
rs1050316 		1 156464911 3 prime UTR variant G/T snv 0.54
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs10908505
rs10908505 		1 156498451 intron variant T/A;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2011 2011
dbSNP: rs10908505
rs10908505 		1 156498451 intron variant T/A;G snv
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs1171563
rs1171563 		1 156486737 intron variant T/G snv 0.21
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		0.700 1.000 1 2016 2016
dbSNP: rs2274319
rs2274319 		1 156481081 intron variant T/C snv 0.62
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2019 2019
dbSNP: rs2274319
rs2274319 		1 156481081 intron variant T/C snv 0.62
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs3790459
rs3790459 		1 156491915 intron variant A/T snv 0.54
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2274316
rs2274316 		0.925 0.040 1 156476450 intron variant C/A snv 0.62 0.54
CUI: C0338480
Disease: Common Migraine
Common Migraine 		Nervous System Diseases 0.020 0.500 2 2017 2017
dbSNP: rs200395694
rs200395694 		1.000 0.080 1 156480799 intron variant G/A;C;T snv 2.7E-05; 1.2E-04; 1.6E-03
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs200395694
rs200395694 		1.000 0.080 1 156480799 intron variant G/A;C;T snv 2.7E-05; 1.2E-04; 1.6E-03
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs2274316
rs2274316 		0.925 0.040 1 156476450 intron variant C/A snv 0.62 0.54
CUI: C0154723
Disease: Migraine with Aura
Migraine with Aura 		Nervous System Diseases 0.010 < 0.001 1 2014 2014