PDYN-AS1, PDYN antisense RNA 1, 727993

N. diseases: 9; N. variants: 22
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: rs1539189
rs1539189 		20 1966633 intron variant A/G snv 2.0E-02
CUI: C1704436
Disease: Peripheral Arterial Diseases
Peripheral Arterial Diseases 		Cardiovascular Diseases 0.700 1.000 1 2016 2016
dbSNP: rs185387034
rs185387034 		20 1970274 intron variant A/G snv 4.6E-03
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
Platelet mean volume determination (procedure) 		0.700 1.000 1 2016 2016
dbSNP: rs4411786
rs4411786 		20 1950251 intron variant T/A;C;G snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs4411786
rs4411786 		20 1950251 intron variant T/A;C;G snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs4618126
rs4618126 		20 1950239 intron variant G/A snv 0.43
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs6035310
rs6035310 		20 2007953 intron variant A/C;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.700 1.000 1 2008 2008
dbSNP: rs6045612
rs6045612 		20 1950355 intron variant C/T snv 0.43
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test) 		0.700 1.000 1 2016 2016
dbSNP: rs6081597
rs6081597 		20 2014888 intron variant A/G snv 2.9E-02
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2235749
rs2235749 		0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2014 2014
dbSNP: rs2235749
rs2235749 		0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37
CUI: C0524662
Disease: Opiate Addiction
Opiate Addiction 		Chemically-Induced Disorders; Mental Disorders 0.010 < 0.001 1 2019 2019
dbSNP: rs2235749
rs2235749 		0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37
CUI: C0024809
Disease: Marijuana Abuse
Marijuana Abuse 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs2235749
rs2235749 		0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs2235749
rs2235749 		0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37
CUI: C0086025
Disease: Codependency
Codependency 		Behavior and Behavior Mechanisms 0.010 1.000 1 2009 2009
dbSNP: rs2235749
rs2235749 		0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		Digestive System Diseases; Neoplasms 0.010 < 0.001 1 2014 2014
dbSNP: rs2235749
rs2235749 		0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37
CUI: C0600427
Disease: Cocaine Dependence
Cocaine Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs1997794
rs1997794 		0.851 0.120 20 1994212 5 prime UTR variant T/C snv 0.50
CUI: C0524662
Disease: Opiate Addiction
Opiate Addiction 		Chemically-Induced Disorders; Mental Disorders 0.030 0.667 3 2009 2019
dbSNP: rs1997794
rs1997794 		0.851 0.120 20 1994212 5 prime UTR variant T/C snv 0.50
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.020 1.000 2 2013 2018
dbSNP: rs910080
rs910080 		0.851 0.120 20 1979580 3 prime UTR variant A/G snv 0.35
CUI: C0524662
Disease: Opiate Addiction
Opiate Addiction 		Chemically-Induced Disorders; Mental Disorders 0.020 1.000 2 2018 2019
dbSNP: rs1997794
rs1997794 		0.851 0.120 20 1994212 5 prime UTR variant T/C snv 0.50
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs1997794
rs1997794 		0.851 0.120 20 1994212 5 prime UTR variant T/C snv 0.50
CUI: C0497327
Disease: Dementia
Dementia 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs910080
rs910080 		0.851 0.120 20 1979580 3 prime UTR variant A/G snv 0.35
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs910080
rs910080 		0.851 0.120 20 1979580 3 prime UTR variant A/G snv 0.35
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs910080
rs910080 		0.851 0.120 20 1979580 3 prime UTR variant A/G snv 0.35
CUI: C0497327
Disease: Dementia
Dementia 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs2235751
rs2235751 		0.882 0.120 20 1989288 intron variant A/G snv 0.40
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.020 1.000 2 2013 2017
dbSNP: rs2235751
rs2235751 		0.882 0.120 20 1989288 intron variant A/G snv 0.40
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2009 2009