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: rs3761847
rs3761847
0.827 0.200 9 120927961 intron variant G/A snv 0.52
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.870 0.909 11 2007 2015
dbSNP: rs2269060
rs2269060
1.000 0.120 9 120921291 intron variant C/T snv 0.52
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 1.000 1 2012 2012
dbSNP: rs1014530
rs1014530
9 120922814 intron variant T/C snv 0.51
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.700 1.000 1 2016 2016
dbSNP: rs2301334
rs2301334
9 120926826 intron variant C/A snv 1.7E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs2416804
rs2416804
9 120914118 intron variant G/C;T snv
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.700 1.000 1 2019 2019
dbSNP: rs3761847
rs3761847
0.827 0.200 9 120927961 intron variant G/A snv 0.52
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.700 1.000 1 2011 2011
dbSNP: rs3761847
rs3761847
0.827 0.200 9 120927961 intron variant G/A snv 0.52
CUI: C0021053
Disease: Immune System Diseases
Immune System Diseases
0.700 1.000 1 2011 2011
dbSNP: rs3761847
rs3761847
0.827 0.200 9 120927961 intron variant G/A snv 0.52
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2011 2011
dbSNP: rs7021206
rs7021206
1.000 0.120 9 120921879 intron variant G/A snv 0.66
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.020 0.500 2 2009 2011
dbSNP: rs2239658
rs2239658
1.000 0.120 9 120909559 intron variant T/C snv 0.69
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.010 1.000 1 2016 2016
dbSNP: rs3761847
rs3761847
0.827 0.200 9 120927961 intron variant G/A snv 0.52
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.010 1.000 1 2012 2012
dbSNP: rs3761847
rs3761847
0.827 0.200 9 120927961 intron variant G/A snv 0.52
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 1.000 1 2009 2009
dbSNP: rs3761847
rs3761847
0.827 0.200 9 120927961 intron variant G/A snv 0.52
CUI: C0338437
Disease: Neurocysticercosis
Neurocysticercosis
0.010 1.000 1 2019 2019
dbSNP: rs3761847
rs3761847
0.827 0.200 9 120927961 intron variant G/A snv 0.52
CUI: C0014544
Disease: Epilepsy
Epilepsy
0.010 1.000 1 2019 2019
dbSNP: rs4836834
rs4836834
1.000 0.120 9 120903623 3 prime UTR variant T/A snv 0.44
CUI: C0018213
Disease: Graves Disease
Graves Disease
0.010 1.000 1 2016 2016