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: rs947583
rs947583 		6 135812521 non coding transcript exon variant T/C snv 0.27
CUI: C0202178
Disease: Phosphorus measurement
Phosphorus measurement 		0.800 1.000 1 2010 2010
dbSNP: rs947583
rs947583 		6 135812521 non coding transcript exon variant T/C snv 0.27
CUI: C0523827
Disease: Inorganic phosphate measurement
Inorganic phosphate measurement 		0.800 1.000 1 2010 2010
dbSNP: rs9494266
rs9494266 		1.000 0.080 6 135530435 intron variant G/A snv 0.27
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.710 0.500 2 2007 2008
dbSNP: rs116990752
rs116990752 		6 135589773 intron variant A/C;G snv 9.3E-03
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs144124553
rs144124553 		6 135539903 intron variant C/T snv 1.0E-02
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2019 2019
dbSNP: rs2327650
rs2327650 		6 135630279 non coding transcript exon variant T/A snv 0.53
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs4895455
rs4895455 		6 135746878 intron variant A/G snv 6.1E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.700 1.000 1 2019 2019
dbSNP: rs761357
rs761357 		0.851 0.040 6 135581461 intron variant A/G;T snv
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2019 2019
dbSNP: rs761357
rs761357 		0.851 0.040 6 135581461 intron variant A/G;T snv
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2019 2019
dbSNP: rs761357
rs761357 		0.851 0.040 6 135581461 intron variant A/G;T snv
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2019 2019
dbSNP: rs761357
rs761357 		0.851 0.040 6 135581461 intron variant A/G;T snv
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		Endocrine System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs761357
rs761357 		0.851 0.040 6 135581461 intron variant A/G;T snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs79846291
rs79846291 		1.000 0.080 6 135756791 intron variant G/A;T snv
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.700 1.000 1 2018 2018
dbSNP: rs9389316
rs9389316 		6 135679865 intron variant C/A;T snv
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7750586
rs7750586 		1.000 0.040 6 135506535 intron variant A/G snv 0.30
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs911507
rs911507 		1.000 0.040 6 135738285 intron variant A/G snv 0.49
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs9647635
rs9647635 		1.000 0.040 6 135519918 intron variant C/A snv 0.70
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 < 0.001 1 2015 2015