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: rs144453041
rs144453041 		1.000 0.040 6 32605248 intergenic variant A/G snv
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		Hemic and Lymphatic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs144660248
rs144660248 		1.000 0.040 6 32583926 intron variant G/T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs144660248
rs144660248 		1.000 0.040 6 32583926 intron variant G/T snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs17191234
rs17191234 		1.000 0.040 6 32596904 intergenic variant A/C snv 0.34
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		Hemic and Lymphatic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs17425622
rs17425622 		1.000 0.040 6 32604184 intergenic variant T/C snv 0.13
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2016 2016
dbSNP: rs2454138
rs2454138 		0.925 0.120 6 32602624 intergenic variant G/A snv 0.27
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs2454138
rs2454138 		0.925 0.120 6 32602624 intergenic variant G/A snv 0.27
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		Hemic and Lymphatic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2454138
rs2454138 		0.925 0.120 6 32602624 intergenic variant G/A snv 0.27
CUI: C0201278
Disease: Antibody measurement (procedure)
Antibody measurement (procedure) 		0.700 1.000 1 2019 2019
dbSNP: rs2516049
rs2516049 		0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		Hemic and Lymphatic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2516049
rs2516049 		0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0030809
Disease: Pemphigus Vulgaris
Pemphigus Vulgaris 		Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2516049
rs2516049 		0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2013 2013
dbSNP: rs2516049
rs2516049 		0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
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: rs2516049
rs2516049 		0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections 		Infections 0.700 1.000 1 2013 2013
dbSNP: rs2516049
rs2516049 		0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2516049
rs2516049 		0.742 0.400 6 32602623 intergenic variant T/C snv 0.27
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.700 1.000 1 2010 2010
dbSNP: rs2516050
rs2516050 		1.000 0.040 6 32602575 intergenic variant G/A snv 0.47
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		Hemic and Lymphatic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2647062
rs2647062 		6 32602640 intergenic variant A/C snv 0.13
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2647071
rs2647071 		1.000 0.040 6 32606133 intergenic variant C/T snv 0.22
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis 		Hemic and Lymphatic Diseases 0.700 1.000 1 2012 2012
dbSNP: rs2647074
rs2647074 		6 32606583 intergenic variant C/T snv 0.30
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2647074
rs2647074 		6 32606583 intergenic variant C/T snv 0.30
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2760981
rs2760981 		1.000 0.040 6 32597688 intergenic variant G/A;C;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs2760981
rs2760981 		1.000 0.040 6 32597688 intergenic variant G/A;C;T snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		Mental Disorders 0.700 1.000 1 2017 2017
dbSNP: rs2760995
rs2760995 		6 32606581 intergenic variant G/A snv 0.20
CUI: C0730345
Disease: Microalbuminuria
Microalbuminuria 		Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2019 2019
dbSNP: rs28366255
rs28366255 		6 32591705 upstream gene variant C/A;T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.700 1.000 1 2018 2018
dbSNP: rs28366266
rs28366266 		6 32591976 upstream gene variant T/C snv 0.12
CUI: C0027726
Disease: Nephrotic Syndrome
Nephrotic Syndrome 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.700 1.000 1 2018 2018