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: rs6062314
rs6062314
0.925 0.160 20 63778360 intron variant C/G;T snv
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.810 1.000 3 2011 2019
dbSNP: rs2315646
rs2315646
1.000 0.080 20 63748397 intron variant T/A;G snv
CUI: C0004096
Disease: Asthma
Asthma
Respiratory Tract Diseases; Immune System Diseases 0.700 1.000 1 2019 2019
dbSNP: rs6010651
rs6010651
20 63786890 intron variant A/C snv 0.43
CUI: C1314691
Disease: Age at menarche
Age at menarche
Behavior and Behavior Mechanisms 0.700 1.000 1 2019 2019
dbSNP: rs6062314
rs6062314
0.925 0.160 20 63778360 intron variant C/G;T snv
CUI: C1367654
Disease: Marginal Zone B-Cell Lymphoma
Marginal Zone B-Cell Lymphoma
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 1 2019 2019
dbSNP: rs6062322
rs6062322
20 63810246 intron variant A/C;T snv 0.20
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs6089970
rs6089970
1.000 0.040 20 63750626 intron variant C/T snv 0.17
CUI: C0013595
Disease: Eczema
Eczema
Skin and Connective Tissue Diseases 0.700 1.000 1 2019 2019
dbSNP: rs73143584
rs73143584
20 63814349 intron variant G/A snv 7.3E-02
CUI: C0005612
Disease: Birth Weight
Birth Weight
Pathological Conditions, Signs and Symptoms 0.700 1.000 1 2019 2019
dbSNP: rs755017
rs755017
0.925 0.080 20 63790269 synonymous variant A/C;G snv 0.17
CUI: C0008707
Disease: Chronic osteomyelitis
Chronic osteomyelitis
Infections; Musculoskeletal Diseases 0.700 0
dbSNP: rs5019252
rs5019252
1.000 0.040 20 63746996 synonymous variant C/T snv 0.34 0.30
CUI: C0017638
Disease: Glioma
Glioma
Neoplasms 0.010 1.000 1 2012 2012
dbSNP: rs755017
rs755017
0.925 0.080 20 63790269 synonymous variant A/C;G snv 0.17
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
Infections 0.010 1.000 1 2019 2019