HDAC4, histone deacetylase 4, 9759

N. diseases: 256; N. variants: 9
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: rs2048765
rs2048765 		2 239286459 intron variant A/G snv 9.6E-02
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		0.700 1.000 2 2018 2018
dbSNP: rs2048765
rs2048765 		2 239286459 intron variant A/G snv 9.6E-02
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.700 1.000 1 2018 2018
dbSNP: rs2100172
rs2100172 		1.000 0.040 2 239062482 intron variant T/C snv 0.15
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs55875066
rs55875066 		0.882 0.080 2 239154306 intron variant C/T snv 6.6E-02
CUI: C0151779
Disease: Cutaneous Melanoma
Cutaneous Melanoma 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2018 2018
dbSNP: rs55875066
rs55875066 		0.882 0.080 2 239154306 intron variant C/T snv 6.6E-02
CUI: C0153536
Disease: Malignant melanoma of skin of lower limb
Malignant melanoma of skin of lower limb 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2018 2018
dbSNP: rs55875066
rs55875066 		0.882 0.080 2 239154306 intron variant C/T snv 6.6E-02
CUI: C0153535
Disease: Malignant melanoma of skin of upper limb
Malignant melanoma of skin of upper limb 		Neoplasms; Skin and Connective Tissue Diseases 0.700 1.000 1 2018 2018
dbSNP: rs9308908
rs9308908 		1.000 0.040 2 239074483 intron variant T/C snv 0.29
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		Neoplasms 0.700 1.000 1 2017 2017
dbSNP: rs1063639
rs1063639 		1.000 0.040 2 239082174 synonymous variant G/A snv 0.54 0.52
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs370963321
rs370963321 		1.000 0.040 2 239134419 missense variant C/T snv 6.0E-04 4.2E-05
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs370963321
rs370963321 		1.000 0.040 2 239134419 missense variant C/T snv 6.0E-04 4.2E-05
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs61754648
rs61754648 		2 239090026 missense variant C/T snv 1.4E-03 1.8E-03
CUI: C0013473
Disease: Eating Disorders
Eating Disorders 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs62182100
rs62182100 		1.000 0.040 2 239283800 intron variant C/G snv 4.3E-02
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs73000144
rs73000144 		0.925 0.080 2 239139704 missense variant C/T snv 3.0E-03 3.2E-03
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2015 2015
dbSNP: rs73000144
rs73000144 		0.925 0.080 2 239139704 missense variant C/T snv 3.0E-03 3.2E-03
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		Neoplasms; Male Urogenital Diseases 0.010 1.000 1 2015 2015