LMOD1, leiomodin 1, 25802

N. diseases: 49; 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: rs2820315
rs2820315 		0.882 0.040 1 201903136 intron variant C/T snv 0.23
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.710 1.000 2 2017 2018
dbSNP: rs2820315
rs2820315 		0.882 0.040 1 201903136 intron variant C/T snv 0.23
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 2 2017 2017
dbSNP: rs17432675
rs17432675 		1.000 0.040 1 201918593 intron variant T/C snv 0.32
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs17432675
rs17432675 		1.000 0.040 1 201918593 intron variant T/C snv 0.32
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs2819368
rs2819368 		1 201941435 intron variant C/T snv 0.98
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2819368
rs2819368 		1 201941435 intron variant C/T snv 0.98
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2819371
rs2819371 		1 201946530 5 prime UTR variant A/C snv 0.92
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2819371
rs2819371 		1 201946530 5 prime UTR variant A/C snv 0.92
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2820300
rs2820300 		1 201939550 intron variant A/G;T snv
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2820300
rs2820300 		1 201939550 intron variant A/G;T snv
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2820301
rs2820301 		1 201943694 intron variant G/A snv 0.96
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2820301
rs2820301 		1 201943694 intron variant G/A snv 0.96
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2820312
rs2820312 		1 201900129 missense variant G/A snv 0.28 0.28
CUI: C1305855
Disease: Body mass index
Body mass index 		0.700 1.000 1 2018 2018
dbSNP: rs2820313
rs2820313 		1 201901093 intron variant A/G snv 0.32
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2019 2019
dbSNP: rs2820315
rs2820315 		0.882 0.040 1 201903136 intron variant C/T snv 0.23
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs34091558
rs34091558 		1.000 0.040 1 201917642 intron variant A/- delins 0.25
CUI: C0425782
Disease: Breast size
Breast size 		0.700 1.000 1 2016 2016
dbSNP: rs777696417
rs777696417 		0.882 0.120 1 201899905 stop gained G/A;C snv
CUI: C2931117
Disease: Fetal megacystis
Fetal megacystis 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2017 2017
dbSNP: rs777696417
rs777696417 		0.882 0.120 1 201899905 stop gained G/A;C snv
CUI: C0266200
Disease: Microcolon
Microcolon 		Digestive System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs777696417
rs777696417 		0.882 0.120 1 201899905 stop gained G/A;C snv
CUI: C0149632
Disease: Abnormality of the bladder
Abnormality of the bladder 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2017 2017
dbSNP: rs777696417
rs777696417 		0.882 0.120 1 201899905 stop gained G/A;C snv
CUI: C0042781
Disease: Visceral Myopathy
Visceral Myopathy 		Digestive System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs2820315
rs2820315 		0.882 0.040 1 201903136 intron variant C/T snv 0.23
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs2820315
rs2820315 		0.882 0.040 1 201903136 intron variant C/T snv 0.23
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2017 2017
dbSNP: rs34091558
rs34091558 		1.000 0.040 1 201917642 intron variant A/- delins 0.25
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2018 2018