Source: ALL

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: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
1.000 0.877 83 2004 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
Diabetes Mellitus, Insulin-Dependent
1.000 0.935 69 2005 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.900 0.955 26 2004 2018
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.870 1.000 8 2005 2018
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.850 1.000 9 2005 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.850 0.600 9 2005 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0677607
Disease: Hashimoto Disease
Hashimoto Disease
0.810 1.000 2 2006 2013
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
0.800 2 2011 2013
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.800 2 2012 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0178468
Disease: Autoimmune thyroid disease
Autoimmune thyroid disease
0.740 1.000 6 2005 2016
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.720 1.000 3 2012 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0033860
Disease: Psoriasis
Psoriasis
0.720 < 0.001 3 2008 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata
0.710 1.000 2 2008 2016
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1 2017 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0004096
Disease: Asthma
Asthma
0.700 1 2011 2011
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1 2017 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1 2017 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing
0.700 1 2017 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1 2017 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
0.700 1 2017 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1 2012 2012
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.700 1 2017 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0750879
Disease: Eosinophil count result
Eosinophil count result
0.700 1 2017 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.700 1 2017 2017
dbSNP: rs2476601
rs2476601
0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92
RHEUMATOID ARTHRITIS, SUSCEPTIBILITY TO
0.700 0