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: rs8022049
rs8022049
14 54996151 intron variant T/C snv 0.30
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.700 1.000 1 2012 2012
dbSNP: rs9285583
rs9285583
14 54964717 intron variant T/C snv 0.43
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.700 1.000 1 2012 2012
dbSNP: rs943914
rs943914
14 54973350 intron variant C/A snv 0.34
CUI: C0202202
Disease: Protein measurement
Protein measurement
0.700 1.000 1 2012 2012
dbSNP: rs774359492
rs774359492
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0949690
Disease: Spondylarthritis
Spondylarthritis
Musculoskeletal Diseases 0.010 1.000 1 2012 2012
dbSNP: rs774359492
rs774359492
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0035435
Disease: Rheumatism
Rheumatism
Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.010 1.000 1 2012 2012
dbSNP: rs774359492
rs774359492
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs774359492
rs774359492
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs774359492
rs774359492
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
Skin and Connective Tissue Diseases 0.010 1.000 1 2012 2012
dbSNP: rs774359492
rs774359492
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases; Stomatognathic Diseases 0.010 1.000 1 2012 2012
dbSNP: rs774359492
rs774359492
0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06
CUI: C0949691
Disease: Spondylarthropathies
Spondylarthropathies
Musculoskeletal Diseases 0.010 1.000 1 2012 2012