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: rs3852257
rs3852257 		1.000 0.080 7 18832069 intron variant C/G;T snv
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs6461386
rs6461386 		1.000 0.080 7 18844067 intron variant G/A;C snv
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs6461387
rs6461387 		1.000 0.080 7 18858682 intron variant G/A snv 0.44
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs6461390
rs6461390 		1.000 0.080 7 18870609 intron variant A/G snv 0.48
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs6461392
rs6461392 		1.000 0.080 7 18873179 intron variant G/A snv 0.47
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs6461393
rs6461393 		1.000 0.080 7 18873192 intron variant T/C;G snv
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs6461394
rs6461394 		1.000 0.080 7 18873267 intron variant C/G;T snv
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs6951144
rs6951144 		1.000 0.080 7 18872166 intron variant C/G snv 0.48
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs6951745
rs6951745 		1.000 0.080 7 18872334 intron variant G/A snv 0.45
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs756853
rs756853 		0.925 0.080 7 18850377 intron variant G/A snv 0.56
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs756854
rs756854 		1.000 0.080 7 18863392 intron variant C/T snv 0.48
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs7794241
rs7794241 		1.000 0.080 7 18873757 intron variant C/A snv 0.39
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs957958
rs957958 		1.000 0.080 7 18837993 intron variant A/G snv 0.41
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs957960
rs957960 		1.000 0.080 7 18837785 intron variant C/A snv 0.42
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2389995
rs2389995 		0.925 0.200 7 18933395 intron variant A/G snv 6.0E-02
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.020 1.000 2 2013 2017
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: rs2023938
rs2023938 		1.000 0.040 7 18997152 3 prime UTR variant T/C snv 0.13
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2240419
rs2240419 		0.925 0.200 7 18935566 intron variant T/A;C snv
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs10248565
rs10248565 		1.000 0.040 7 18935100 intron variant T/G snv 0.14
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder) 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs10248565
rs10248565 		1.000 0.040 7 18935100 intron variant T/G snv 0.14
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs10248565
rs10248565 		1.000 0.040 7 18935100 intron variant T/G snv 0.14
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs10269422
rs10269422 		7 18814978 intron variant T/A snv 0.46
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014
dbSNP: rs12540872
rs12540872 		7 18797044 intron variant G/A;T snv
CUI: C0027651
Disease: Neoplasms
Neoplasms 		Neoplasms 0.010 1.000 1 2014 2014
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