HDAC9, histone deacetylase 9, 9734

N. diseases: 340; N. variants: 73
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: rs1178326
rs1178326 		1.000 0.040 7 18195234 intron variant T/C snv 3.9E-02
CUI: C0423791
Disease: Maculopapular Lesion
Maculopapular Lesion 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs1178326
rs1178326 		1.000 0.040 7 18195234 intron variant T/C snv 3.9E-02
CUI: C0014544
Disease: Epilepsy
Epilepsy 		Nervous System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs1528683
rs1528683 		7 18196884 intron variant C/G snv 7.9E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs302152
rs302152 		1.000 0.040 7 18224045 intron variant A/T snv 0.61
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs302153
rs302153 		7 18227606 intron variant G/A snv 0.77
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs302147
rs302147 		1.000 0.080 7 18245750 intron variant C/T snv 0.78
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2009 2009
dbSNP: rs11764536
rs11764536 		1.000 0.040 7 18370370 intron variant A/C snv 1.4E-02
CUI: C0029410
Disease: Osteoarthritis of hip
Osteoarthritis of hip 		Musculoskeletal Diseases 0.700 1.000 1 2018 2018
dbSNP: rs12155400
rs12155400 		7 18389298 intron variant A/G snv 2.9E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs12155400
rs12155400 		7 18389298 intron variant A/G snv 2.9E-02
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases 		Eye Diseases 0.010 1.000 1 2013 2013
dbSNP: rs61549860
rs61549860 		1.000 0.040 7 18404796 intron variant A/G;T snv
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.700 1.000 1 2016 2016
dbSNP: rs17432268
rs17432268 		7 18446819 intron variant A/G snv 6.0E-03
CUI: C0678909
Disease: Brain Waves
Brain Waves 		0.700 1.000 1 2019 2019
dbSNP: rs213273
rs213273 		1.000 7 18464885 intron variant G/A snv 0.96
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.700 1.000 1 2014 2014
dbSNP: rs213273
rs213273 		1.000 7 18464885 intron variant G/A snv 0.96
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.700 1.000 1 2014 2014
dbSNP: rs213273
rs213273 		1.000 7 18464885 intron variant G/A snv 0.96
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.700 1.000 1 2014 2014
dbSNP: rs213273
rs213273 		1.000 7 18464885 intron variant G/A snv 0.96
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.700 1.000 1 2014 2014
dbSNP: rs213273
rs213273 		1.000 7 18464885 intron variant G/A snv 0.96
CUI: C0442874
Disease: Neuropathy
Neuropathy 		Nervous System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs17347800
rs17347800 		7 18477656 intron variant G/A;T snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.700 1.000 1 2015 2015
dbSNP: rs1233806222
rs1233806222 		1.000 0.080 7 18585444 synonymous variant G/A snv 1.4E-05
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		Nutritional and Metabolic Diseases; Nervous System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs779782995
rs779782995 		0.925 0.040 7 18590438 missense variant A/G snv 1.7E-05
CUI: C4551472
Disease: Hypertrophic obstructive cardiomyopathy
Hypertrophic obstructive cardiomyopathy 		Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs779782995
rs779782995 		0.925 0.040 7 18590438 missense variant A/G snv 1.7E-05
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs1161136341
rs1161136341 		0.925 0.080 7 18591621 missense variant G/A snv 8.0E-06 1.4E-05
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		Neoplasms 0.010 1.000 1 2019 2019
dbSNP: rs1161136341
rs1161136341 		0.925 0.080 7 18591621 missense variant G/A snv 8.0E-06 1.4E-05
CUI: C0153633
Disease: Malignant neoplasm of brain
Malignant neoplasm of brain 		Neoplasms; Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs76872642
rs76872642 		7 18629780 intron variant G/A snv 5.0E-03
CUI: C0684328
Disease: Reasoning
Reasoning 		0.700 1.000 1 2018 2018
dbSNP: rs774238794
rs774238794 		0.925 0.080 7 18644690 missense variant G/A;T snv 4.1E-05; 4.1E-06
CUI: C0153633
Disease: Malignant neoplasm of brain
Malignant neoplasm of brain 		Neoplasms; Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs774238794
rs774238794 		0.925 0.080 7 18644690 missense variant G/A;T snv 4.1E-05; 4.1E-06
CUI: C1621958
Disease: Glioblastoma Multiforme
Glioblastoma Multiforme 		Neoplasms 0.010 1.000 1 2019 2019