Source: GWASDB

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: rs3817973
rs3817973
0.925 0.200 6 32393334 intron variant C/T snv 0.39
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 2 2007 2011
dbSNP: rs3817973
rs3817973
0.925 0.200 6 32393334 intron variant C/T snv 0.39
Diabetes Mellitus, Insulin-Dependent
0.700 1.000 1 2007 2007
dbSNP: rs3129953
rs3129953
1.000 0.120 6 32394044 synonymous variant C/T snv 0.10 0.13
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs1980493
rs1980493
0.776 0.400 6 32395438 intron variant T/C snv 0.13
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 3 2007 2011
dbSNP: rs1980493
rs1980493
0.776 0.400 6 32395438 intron variant T/C snv 0.13
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 1.000 1 2014 2014
dbSNP: rs1980493
rs1980493
0.776 0.400 6 32395438 intron variant T/C snv 0.13
CUI: C0338451
Disease: Frontotemporal dementia
Frontotemporal dementia
0.700 1.000 1 2014 2014
dbSNP: rs1980493
rs1980493
0.776 0.400 6 32395438 intron variant T/C snv 0.13
Diabetes Mellitus, Insulin-Dependent
0.800 1.000 1 2007 2015
dbSNP: rs1980493
rs1980493
0.776 0.400 6 32395438 intron variant T/C snv 0.13
CUI: C0026896
Disease: Myasthenia Gravis
Myasthenia Gravis
0.700 1.000 1 2012 2012
dbSNP: rs1980493
rs1980493
0.776 0.400 6 32395438 intron variant T/C snv 0.13
Anti-cyclic citrullinated peptide antibody
0.700 1.000 1 2009 2009
dbSNP: rs2076533
rs2076533
0.882 0.200 6 32395750 intron variant C/T snv 0.40
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs2076533
rs2076533
0.882 0.200 6 32395750 intron variant C/T snv 0.40
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2007 2007
dbSNP: rs2076533
rs2076533
0.882 0.200 6 32395750 intron variant C/T snv 0.40
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs2076531
rs2076531
1.000 0.040 6 32395935 intron variant A/G;T snv
CUI: C4021107
Disease: Non-obstructive azoospermia
Non-obstructive azoospermia
0.700 1.000 1 2012 2012
dbSNP: rs2076530
rs2076530
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.710 1.000 3 2005 2011
dbSNP: rs2076530
rs2076530
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40
Diabetes Mellitus, Insulin-Dependent
0.710 1.000 1 2005 2007
dbSNP: rs2076530
rs2076530
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs2076530
rs2076530
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2007 2007
dbSNP: rs2076530
rs2076530
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.900 0.933 1 2005 2019
dbSNP: rs9268480
rs9268480
0.882 0.200 6 32396067 synonymous variant C/T snv 0.26 0.24
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2007 2007
dbSNP: rs9268480
rs9268480
0.882 0.200 6 32396067 synonymous variant C/T snv 0.26 0.24
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 1.000 1 2012 2012
dbSNP: rs9268480
rs9268480
0.882 0.200 6 32396067 synonymous variant C/T snv 0.26 0.24
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs2076529
rs2076529
1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2007 2007
dbSNP: rs2076529
rs2076529
1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.800 1.000 1 2010 2010
dbSNP: rs9268481
rs9268481
1.000 0.040 6 32396579 intron variant A/G snv 0.24
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 1.000 1 2012 2012
dbSNP: rs3129954
rs3129954
1.000 0.120 6 32397803 intron variant A/G snv 0.72
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011