MEIS1, Meis homeobox 1, 4211

N. diseases: 104; N. variants: 19
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: rs2300478
rs2300478 		0.851 0.120 2 66554321 intron variant T/G snv 0.21
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		Nervous System Diseases; Mental Disorders 0.820 1.000 4 2007 2016
dbSNP: rs3891585
rs3891585 		2 66529844 intron variant A/C;G snv
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.800 1.000 3 2011 2019
dbSNP: rs10865355
rs10865355 		2 66537865 intron variant A/G snv 0.61
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.800 1.000 2 2011 2019
dbSNP: rs11897119
rs11897119 		2 66544868 intron variant T/A;C snv
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.800 1.000 2 2010 2019
dbSNP: rs113851554
rs113851554 		0.882 0.080 2 66523432 intron variant G/A;T snv
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 2 2017 2018
dbSNP: rs113851554
rs113851554 		0.882 0.080 2 66523432 intron variant G/A;T snv
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms 		0.700 1.000 2 2017 2018
dbSNP: rs2300481
rs2300481 		2 66555335 intron variant C/T snv 0.36
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.700 1.000 2 2018 2019
dbSNP: rs113851554
rs113851554 		0.882 0.080 2 66523432 intron variant G/A;T snv
CUI: C0021603
Disease: Sleep Initiation and Maintenance Disorders
Sleep Initiation and Maintenance Disorders 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs113851554
rs113851554 		0.882 0.080 2 66523432 intron variant G/A;T snv
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs11677371
rs11677371 		2 66529281 intron variant A/G;T snv
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2011 2011
dbSNP: rs11692361
rs11692361 		1.000 0.040 2 66496567 intron variant C/G;T snv
CUI: C0014175
Disease: Endometriosis
Endometriosis 		Female Urogenital Diseases and Pregnancy Complications 0.700 1.000 1 2017 2017
dbSNP: rs11897119
rs11897119 		2 66544868 intron variant T/A;C snv
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs11897119
rs11897119 		2 66544868 intron variant T/A;C snv
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs12469063
rs12469063 		0.925 0.080 2 66537176 intron variant A/G snv 0.18
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2007 2007
dbSNP: rs13033745
rs13033745 		2 66433271 intron variant G/T snv 0.67
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs13033745
rs13033745 		2 66433271 intron variant G/T snv 0.67
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs1519104
rs1519104 		2 66453760 intron variant G/A snv 0.68
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2280334
rs2280334 		2 66438014 intron variant T/C snv 0.60
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2280334
rs2280334 		2 66438014 intron variant T/C snv 0.60
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2300481
rs2300481 		2 66555335 intron variant C/T snv 0.36
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		0.700 1.000 1 2017 2017
dbSNP: rs4430933
rs4430933 		2 66522478 intron variant A/G snv 0.58
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2018 2018
dbSNP: rs4433986
rs4433986 		2 66533179 intron variant A/G snv 0.59
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2011 2011
dbSNP: rs62144050
rs62144050 		2 66497930 intron variant T/C snv 0.28
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		0.700 1.000 1 2016 2016
dbSNP: rs6724747
rs6724747 		2 66522696 intron variant G/A snv 0.23
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2019 2019
dbSNP: rs7603236
rs7603236 		2 66535279 intron variant C/T snv 0.61
CUI: C0429087
Disease: Electrocardiogram: P-R interval
Electrocardiogram: P-R interval 		0.700 1.000 1 2011 2011