Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs12722547
rs12722547
10 6030130 intron variant G/C snv 7.8E-03
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases
0.700 1.000 1 2019 2019
dbSNP: rs3118469
rs3118469
10 6059166 intron variant A/T snv 0.24
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs4747846
rs4747846
10 6032488 intron variant G/A;C;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2017 2017
dbSNP: rs7090504
rs7090504
10 6049054 intron variant T/A snv 0.16
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.900 1.000 2 2007 2019
dbSNP: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1.000 1 2016 2016
dbSNP: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2016 2016
dbSNP: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.830 1.000 1 2012 2015
dbSNP: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 1.000 1 2016 2016
dbSNP: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2016 2016
dbSNP: rs2104286
rs2104286
0.662 0.440 10 6057082 intron variant T/C snv 0.18
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2016 2016
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 1.000 3 2010 2019
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.810 0.750 2 2011 2019
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
0.700 1.000 2 2015 2019
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
0.700 1.000 2 2015 2019
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
0.700 1.000 2 2015 2019
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency
0.700 1.000 1 2015 2015
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2015 2015
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis
0.700 1.000 1 2015 2015
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.700 1.000 1 2015 2015
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1.000 1 2015 2015
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.700 1.000 1 2015 2015
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
Diabetes Mellitus, Insulin-Dependent
0.750 1.000 1 2007 2015
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis
0.700 1.000 1 2015 2015
dbSNP: rs706778
rs706778
0.695 0.320 10 6056986 intron variant C/T snv 0.46
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.700 1.000 1 2015 2015