SKIV2L, Ski2 like RNA helicase, 6499

N. diseases: 96; N. variants: 24
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: rs429608
rs429608
0.851 0.160 6 31962685 intron variant G/A snv 0.14 0.16
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
Eye Diseases 0.870 1.000 12 2010 2019
dbSNP: rs281875237
rs281875237
1.000 6 31962012 missense variant T/G snv
CUI: C3281289
Disease: TRICHOHEPATOENTERIC SYNDROME 2
TRICHOHEPATOENTERIC SYNDROME 2
0.800 1.000 1 2012 2012
dbSNP: rs406936
rs406936
0.882 0.240 6 31965384 intron variant G/A snv 0.19
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
Eye Diseases 0.800 1.000 1 2013 2013
dbSNP: rs406936
rs406936
0.882 0.240 6 31965384 intron variant G/A snv 0.19
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 3 2007 2011
dbSNP: rs438999
rs438999
0.925 0.160 6 31960529 missense variant A/G snv 9.7E-02 0.12
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 3 2007 2011
dbSNP: rs454212
rs454212
0.925 0.200 6 31966595 intron variant C/T snv 0.19
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 3 2007 2011
dbSNP: rs116503776
rs116503776
0.827 0.040 6 31962685 intron variant G/A snv
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
Eye Diseases 0.700 1.000 2 2016 2018
dbSNP: rs437179
rs437179
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 2 2007 2009
dbSNP: rs114212579
rs114212579
1.000 0.080 6 31968280 non coding transcript exon variant G/T snv
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic
Skin and Connective Tissue Diseases; Musculoskeletal Diseases 0.700 1.000 1 2019 2019
dbSNP: rs115566560
rs115566560
6 31964400 intron variant C/T snv
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs116503776
rs116503776
0.827 0.040 6 31962685 intron variant G/A snv
CUI: C1536085
Disease: Geographic Atrophy
Geographic Atrophy
Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs116503776
rs116503776
0.827 0.040 6 31962685 intron variant G/A snv
CUI: C2237660
Disease: exudative macular degeneration
exudative macular degeneration
Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs116503776
rs116503776
0.827 0.040 6 31962685 intron variant G/A snv
Exudative age-related macular degeneration
Eye Diseases 0.700 1.000 1 2016 2016
dbSNP: rs34241101
rs34241101
1.000 6 31968280 non coding transcript exon variant G/T snv 7.2E-02 8.7E-02
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 1.000 1 2010 2010
dbSNP: rs34241101
rs34241101
1.000 6 31968280 non coding transcript exon variant G/T snv 7.2E-02 8.7E-02
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.700 1.000 1 2010 2010
dbSNP: rs34241101
rs34241101
1.000 6 31968280 non coding transcript exon variant G/T snv 7.2E-02 8.7E-02
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.700 1.000 1 2010 2010
dbSNP: rs34241101
rs34241101
1.000 6 31968280 non coding transcript exon variant G/T snv 7.2E-02 8.7E-02
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 1.000 1 2010 2010
dbSNP: rs401775
rs401775
1.000 6 31963360 intron variant T/C snv 0.23
CUI: C1836233
Disease: AIDS, PROGRESSION TO
AIDS, PROGRESSION TO
0.700 1.000 1 2010 2010
dbSNP: rs401775
rs401775
1.000 6 31963360 intron variant T/C snv 0.23
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
0.700 1.000 1 2010 2010
dbSNP: rs401775
rs401775
1.000 6 31963360 intron variant T/C snv 0.23
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO
0.700 1.000 1 2010 2010
dbSNP: rs401775
rs401775
1.000 6 31963360 intron variant T/C snv 0.23
CUI: C1836231
Disease: HIV-1, RESISTANCE TO
HIV-1, RESISTANCE TO
0.700 1.000 1 2010 2010
dbSNP: rs406936
rs406936
0.882 0.240 6 31965384 intron variant G/A snv 0.19
Diabetes Mellitus, Insulin-Dependent
Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.700 1.000 1 2007 2007
dbSNP: rs419788
rs419788
1.000 0.120 6 31961022 intron variant T/A;C snv 0.76
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.700 1.000 1 2011 2011
dbSNP: rs437179
rs437179
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
Skin and Connective Tissue Diseases; Immune System Diseases 0.700 1.000 1 2014 2014
dbSNP: rs437179
rs437179
0.882 0.160 6 31961237 missense variant A/C snv 0.76 0.78
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
Immune System Diseases; Nervous System Diseases 0.700 1.000 1 2010 2010