SNHG32, small nucleolar RNA host gene 32, 50854

N. diseases: 12; N. variants: 4
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: rs9368699
rs9368699 		0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO 		0.800 1.000 2 2009 2010
dbSNP: rs9368699
rs9368699 		0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO 		0.800 1.000 2 2009 2010
dbSNP: rs9368699
rs9368699 		0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		0.800 1.000 2 2009 2010
dbSNP: rs9368699
rs9368699 		0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02
CUI: C1836230
Disease: HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		0.800 1.000 2 2009 2010
dbSNP: rs115487693
rs115487693 		6 31837823 intron variant T/C snv 5.0E-02
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs17201248
rs17201248 		0.925 0.160 6 31835353 non coding transcript exon variant C/G;T snv 4.3E-06; 2.8E-02
CUI: C0018213
Disease: Graves Disease
Graves Disease 		Eye Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs17201248
rs17201248 		0.925 0.160 6 31835353 non coding transcript exon variant C/G;T snv 4.3E-06; 2.8E-02
CUI: C0272178
Disease: Drug-induced neutropenia
Drug-induced neutropenia 		Hemic and Lymphatic Diseases 0.700 1.000 1 2015 2015
dbSNP: rs3130679
rs3130679 		1.000 0.120 6 31839763 non coding transcript exon variant A/G snv 6.4E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs9368699
rs9368699 		0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2013 2013
dbSNP: rs9368699
rs9368699 		0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs9368699
rs9368699 		0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		Infections; Immune System Diseases 0.700 1.000 1 2009 2009
dbSNP: rs9368699
rs9368699 		0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02
CUI: C0033860
Disease: Psoriasis
Psoriasis 		Skin and Connective Tissue Diseases 0.010 1.000 1 2017 2017