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: rs2701448
rs2701448 		8 72096014 intron variant C/A;T snv 8.2E-02
CUI: C0233849
Disease: Personality Traits
Personality Traits 		Behavior and Behavior Mechanisms 0.700 1.000 1 2013 2013
dbSNP: rs398123010
rs398123010 		0.882 0.040 8 72034369 missense variant T/C snv
CUI: C3808667
Disease: EPISODIC PAIN SYNDROME, FAMILIAL, 1
EPISODIC PAIN SYNDROME, FAMILIAL, 1 		0.700 1.000 1 2010 2010
dbSNP: rs11988795
rs11988795 		8 72037366 intron variant C/G;T snv
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2014 2014
dbSNP: rs1384001
rs1384001 		1.000 0.080 8 72024002 intron variant C/A snv 0.48
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs200192163
rs200192163 		8 72036453 missense variant C/A;G snv 1.6E-05
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2014 2014
dbSNP: rs3735945
rs3735945 		1.000 0.080 8 72062571 intron variant C/T snv 0.16
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs398123010
rs398123010 		0.882 0.040 8 72034369 missense variant T/C snv
CUI: C0391976
Disease: Pain Disorder
Pain Disorder 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs398123010
rs398123010 		0.882 0.040 8 72034369 missense variant T/C snv
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 1.000 1 2014 2014
dbSNP: rs4738202
rs4738202 		1.000 0.080 8 72028626 intron variant A/G snv 0.68
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs7010969
rs7010969 		1.000 0.080 8 72070130 intron variant A/C snv 0.69
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs920829
rs920829 		0.925 0.160 8 72065468 missense variant C/T snv 0.14 0.16
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs920829
rs920829 		0.925 0.160 8 72065468 missense variant C/T snv 0.14 0.16
CUI: C0085625
Disease: Hypoalgesia
Hypoalgesia 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs920829
rs920829 		0.925 0.160 8 72065468 missense variant C/T snv 0.14 0.16
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs959974
rs959974 		1.000 0.080 8 72023604 intron variant G/T snv 0.48
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2017 2017