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: rs12194442
rs12194442 		6 24866267 intron variant A/G snv 4.7E-02
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012
dbSNP: rs186361153
rs186361153 		6 24992134 intron variant A/G;T snv
CUI: C3548479
Disease: response to bronchodilator
response to bronchodilator 		0.700 1.000 1 2015 2015
dbSNP: rs680009
rs680009 		1.000 0.120 6 24950601 intron variant A/G snv 0.54
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2009 2009
dbSNP: rs6911302
rs6911302 		6 24819824 intron variant A/C snv 0.46
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement 		0.700 1.000 1 2016 2016
dbSNP: rs79014439
rs79014439 		1.000 0.080 6 24901633 intron variant T/C snv 3.4E-02
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2015 2015
dbSNP: rs875989828
rs875989828 		1.000 6 24873800 splice acceptor variant C/T snv
CUI: C4225298
Disease: DEAFNESS, AUTOSOMAL RECESSIVE 104
DEAFNESS, AUTOSOMAL RECESSIVE 104 		0.700 0
dbSNP: rs10946737
rs10946737 		6 24967012 intron variant G/A snv 0.27
CUI: C0860207
Disease: Drug-Induced Liver Disease
Drug-Induced Liver Disease 		Digestive System Diseases; Chemically-Induced Disorders 0.010 1.000 1 2019 2019
dbSNP: rs9393597
rs9393597 		0.925 0.080 6 24972880 intron variant A/G snv 0.15
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs9393597
rs9393597 		0.925 0.080 6 24972880 intron variant A/G snv 0.15
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		Neoplasms; Skin and Connective Tissue Diseases 0.010 < 0.001 1 2012 2012