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: rs3104373
rs3104373
0.925 0.120 6 32632598 intron variant T/C snv 0.85
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.700 1.000 1 2016 2016
dbSNP: rs28798705
rs28798705
1.000 0.080 6 32650032 downstream gene variant A/G snv 0.66
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs3104367
rs3104367
1.000 0.080 6 32635710 intron variant T/C snv 0.57
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2016 2016
dbSNP: rs9272105
rs9272105
0.925 0.120 6 32632222 intron variant G/A snv 0.55
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.810 1.000 1 2012 2015
dbSNP: rs9272346
rs9272346
0.790 0.320 6 32636595 intron variant G/A snv 0.54
CUI: C0004096
Disease: Asthma
Asthma
0.810 1.000 4 2012 2019
dbSNP: rs9272346
rs9272346
0.790 0.320 6 32636595 intron variant G/A snv 0.54
Diabetes Mellitus, Insulin-Dependent
0.810 1.000 2 2007 2015
dbSNP: rs9272346
rs9272346
0.790 0.320 6 32636595 intron variant G/A snv 0.54
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs9272346
rs9272346
0.790 0.320 6 32636595 intron variant G/A snv 0.54
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma
0.700 1.000 1 2019 2019
dbSNP: rs17843604
rs17843604
0.925 0.120 6 32652506 intergenic variant C/T snv 0.49
CUI: C0004096
Disease: Asthma
Asthma
0.800 1.000 1 2010 2019
dbSNP: rs9272143
rs9272143
0.882 0.080 6 32633026 intron variant T/C snv 0.49
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma
0.720 1.000 2 2013 2017
dbSNP: rs9273123
rs9273123
1.000 0.080 6 32644956 non coding transcript exon variant G/A snv 0.46
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs6927022
rs6927022
1.000 0.040 6 32644620 non coding transcript exon variant A/G snv 0.42
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.800 1.000 2 2012 2017
dbSNP: rs6927022
rs6927022
1.000 0.040 6 32644620 non coding transcript exon variant A/G snv 0.42
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.700 1.000 1 2017 2017
dbSNP: rs1048372
rs1048372
6 32642659 synonymous variant T/C snv 0.63 0.34
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs9272219
rs9272219
0.925 0.160 6 32634492 intron variant G/T snv 0.29
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.800 1.000 1 2009 2009
dbSNP: rs9272975
rs9272975
6 32643544 3 prime UTR variant T/A snv 0.29
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs2040406
rs2040406
0.882 0.240 6 32635230 intron variant A/G snv 0.23
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 1.000 1 2010 2010
dbSNP: rs4455710
rs4455710
1.000 0.040 6 32641081 intron variant C/T snv 0.22
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.700 1.000 1 2016 2016
dbSNP: rs200930495
rs200930495
6 32644683 non coding transcript exon variant G/A snv 0.22
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs28755170
rs28755170
6 32654355 regulatory region variant G/A snv 0.19
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.700 1.000 1 2018 2018
dbSNP: rs3129769
rs3129769
1.000 0.120 6 32629245 intron variant G/A snv 0.15
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 1.000 1 2016 2016
dbSNP: rs28383364
rs28383364
1.000 0.080 6 32639135 3 prime UTR variant A/G snv 0.11
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs13214992
rs13214992
6 32632808 5 prime UTR variant G/A snv 6.9E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs146668528
rs146668528
1.000 0.080 6 32630251 intron variant C/T snv 5.7E-02
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2018 2018
dbSNP: rs146668528
rs146668528
1.000 0.080 6 32630251 intron variant C/T snv 5.7E-02
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2018 2018