LRRK2-DT, LRRK2 divergent transcript, 107984474

N. diseases: 6; 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: rs11175593
rs11175593 		0.882 0.160 12 40208138 non coding transcript exon variant C/T snv 2.8E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.820 1.000 3 2008 2013
dbSNP: rs76904798
rs76904798 		0.925 0.080 12 40220632 intron variant C/T snv 0.13
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.710 1.000 3 2014 2017
dbSNP: rs11175593
rs11175593 		0.882 0.160 12 40208138 non coding transcript exon variant C/T snv 2.8E-02
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs11175593
rs11175593 		0.882 0.160 12 40208138 non coding transcript exon variant C/T snv 2.8E-02
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs11564273
rs11564273 		1.000 0.040 12 40204350 intron variant T/G snv 6.5E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs1907631
rs1907631 		12 40212861 intron variant T/C snv 8.5E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1907631
rs1907631 		12 40212861 intron variant T/C snv 8.5E-02
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
Low density lipoprotein cholesterol measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2046932
rs2046932 		1.000 0.040 12 40186638 intron variant G/A snv 4.8E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs10878226
rs10878226 		1.000 0.040 12 40223890 non coding transcript exon variant G/A;C snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs117762348
rs117762348 		1.000 0.040 12 40203810 non coding transcript exon variant A/G snv 6.5E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1491923
rs1491923 		1.000 0.040 12 40197315 intron variant A/G snv 0.35
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2009 2009
dbSNP: rs2638272
rs2638272 		1.000 0.080 12 40216081 intron variant G/A snv 0.58
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs76904798
rs76904798 		0.925 0.080 12 40220632 intron variant C/T snv 0.13
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.010 1.000 1 2017 2017