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: 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: rs10947262
rs10947262
0.925 0.040 6 32405535 non coding transcript exon variant C/T snv 0.12
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
0.810 1.000 1 2010 2010
dbSNP: rs3817963
rs3817963
0.776 0.360 6 32400310 intron variant T/C snv 0.25
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
0.810 1.000 1 2012 2017
dbSNP: rs3763309
rs3763309
0.882 0.160 6 32408196 upstream gene variant C/A;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 1.000 2 2007 2014
dbSNP: rs3806156
rs3806156
0.827 0.280 6 32405921 intron variant G/A;T snv
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 1.000 2 2010 2012
dbSNP: rs10947261
rs10947261
0.882 0.240 6 32405455 splice region variant G/T snv 0.11
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.800 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: 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: rs3763309
rs3763309
0.882 0.160 6 32408196 upstream gene variant C/A;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.800 1.000 1 2011 2018
dbSNP: rs3763317
rs3763317
1.000 0.040 6 32409011 upstream gene variant C/T snv 0.49
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure)
0.800 1.000 1 2012 2012
dbSNP: rs3817963
rs3817963
0.776 0.360 6 32400310 intron variant T/C snv 0.25
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1.000 1 2013 2013
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: rs3817963
rs3817963
0.776 0.360 6 32400310 intron variant T/C snv 0.25
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.710 1.000 1 2012 2013
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: rs3806156
rs3806156
0.827 0.280 6 32405921 intron variant G/A;T snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 3 2007 2011
dbSNP: rs3817963
rs3817963
0.776 0.360 6 32400310 intron variant T/C snv 0.25
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 3 2007 2011
dbSNP: rs3763305
rs3763305
1.000 0.120 6 32401711 intron variant G/A snv 4.6E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 2 2007 2009
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: rs9268492
rs9268492
0.882 0.200 6 32407503 non coding transcript exon variant C/G snv 0.31
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 2 2007 2011
dbSNP: rs9268494
rs9268494
0.882 0.200 6 32407575 non coding transcript exon variant A/C;T snv 0.32
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 2 2007 2011
dbSNP: rs10947260
rs10947260
1.000 0.120 6 32405408 intron variant T/C snv 0.11 0.11
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011
dbSNP: rs10947261
rs10947261
0.882 0.240 6 32405455 splice region variant G/T snv 0.11
CUI: C0149678
Disease: Epstein-Barr Virus Infections
Epstein-Barr Virus Infections
0.700 1.000 1 2013 2013
dbSNP: rs10947261
rs10947261
0.882 0.240 6 32405455 splice region variant G/T snv 0.11
CUI: C0027404
Disease: Narcolepsy
Narcolepsy
0.700 1.000 1 2009 2009
dbSNP: rs10947261
rs10947261
0.882 0.240 6 32405455 splice region variant G/T snv 0.11
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2011 2011