Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
47 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 0.800 1.000 2 2013 2016
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 0.040 1.000 4 2015 2019
Neuromyelitis Optica
CUI: C0027873
Disease: Neuromyelitis Optica
45 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 0.020 1.000 2 2019 2019
Primary Sjögren's syndrome
CUI: C0151449
Disease: Primary Sjögren's syndrome
42 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 0.020 1.000 2 2013 2019
Chromosome 11p11.2 Deletion Syndrome
CUI: C1832588
Disease: Chromosome 11p11.2 Deletion Syndrome
6 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 0.010 1.000 1 2016 2016
Lupus Nephritis
CUI: C0024143
Disease: Lupus Nephritis
64 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 0.010 1.000 1 2019 2019
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 0.010 1.000 1 2019 2019
PEELING SKIN SYNDROME
CUI: C1849193
Disease: PEELING SKIN SYNDROME
11 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 0.010 1.000 1 2016 2016
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 0.010 1.000 1 2019 2019
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 0.010 1.000 1 2016 2016