KLF12, Kruppel like factor 12, 11278

N. diseases: 58; N. variants: 20
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: rs12429889
rs12429889 		13 74168185 intergenic variant T/C snv 0.29
CUI: C1720824
Disease: Sudden Cardiac Arrest
Sudden Cardiac Arrest 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs12429889
rs12429889 		13 74168185 intergenic variant T/C snv 0.29
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs12877581
rs12877581 		1.000 0.040 13 73751362 intron variant G/C snv 0.19
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2015 2015
dbSNP: rs1324913
rs1324913 		13 74061451 intergenic variant G/T snv 0.39
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2014 2014
dbSNP: rs1886512
rs1886512 		13 73946049 intron variant T/A snv 0.40
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		0.700 1.000 1 2016 2016
dbSNP: rs1886512
rs1886512 		13 73946049 intron variant T/A snv 0.40
CUI: C0018803
Disease: Heart Function Tests
Heart Function Tests 		0.700 1.000 1 2010 2010
dbSNP: rs2025424
rs2025424 		0.925 0.040 13 73724729 intron variant A/G snv 0.16
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs2025424
rs2025424 		0.925 0.040 13 73724729 intron variant A/G snv 0.16
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs2325562
rs2325562 		1.000 0.080 13 73772955 intron variant G/T snv 1.00
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs35185444
rs35185444 		13 74143171 intergenic variant T/C snv 0.18
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs4454843
rs4454843 		13 73974964 intron variant T/C snv 0.34
CUI: C0005890
Disease: Body Height
Body Height 		0.700 1.000 1 2019 2019
dbSNP: rs58598658
rs58598658 		0.925 0.080 13 73887725 intron variant -/A;AA delins
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs58598658
rs58598658 		0.925 0.080 13 73887725 intron variant -/A;AA delins
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs58598658
rs58598658 		0.925 0.080 13 73887725 intron variant -/A;AA delins
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs58598658
rs58598658 		0.925 0.080 13 73887725 intron variant -/A;AA delins
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		Chemically-Induced Disorders 0.700 1.000 1 2017 2017
dbSNP: rs66504755
rs66504755 		13 74128404 intergenic variant AA/-;A delins 0.55
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs728926
rs728926 		13 73938985 intron variant C/T snv 0.34
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		0.700 1.000 1 2014 2014
dbSNP: rs728926
rs728926 		13 73938985 intron variant C/T snv 0.34
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		0.700 1.000 1 2016 2016
dbSNP: rs7329599
rs7329599 		13 73987569 intron variant C/A;G;T snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs7335976
rs7335976 		13 74127968 intergenic variant C/T snv 0.22
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs7995668
rs7995668 		13 74131042 intergenic variant A/C;G snv
CUI: C1314691
Disease: Age at menarche
Age at menarche 		Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs7995760
rs7995760 		0.925 0.040 13 74114584 regulatory region variant T/A;G snv
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.700 1.000 1 2018 2018
dbSNP: rs7995760
rs7995760 		0.925 0.040 13 74114584 regulatory region variant T/A;G snv
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs9318213
rs9318213 		1.000 0.040 13 73763081 intron variant T/C snv 0.43
CUI: C1863416
Disease: Autosomal dominant compelling helio ophthalmic outburst syndrome
Autosomal dominant compelling helio ophthalmic outburst syndrome 		Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2016 2016
dbSNP: rs9600233
rs9600233 		13 74119264 intergenic variant G/A snv 0.13
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019