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: rs1012793
rs1012793
5 132445653 intron variant G/A;C snv
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
0.700 1.000 1 2017 2017
dbSNP: rs3749833
rs3749833
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2017 2017
dbSNP: rs7734334
rs7734334
5 132479312 intron variant C/A snv 0.38
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure
0.700 1.000 1 2017 2017
dbSNP: rs2522061
rs2522061
5 132468353 intron variant G/T snv 0.24
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs2522061
rs2522061
5 132468353 intron variant G/T snv 0.24
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs2548992
rs2548992
1.000 0.080 5 132472976 non coding transcript exon variant A/G;T snv
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2018 2018
dbSNP: rs2548992
rs2548992
1.000 0.080 5 132472976 non coding transcript exon variant A/G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
0.700 1.000 1 2018 2018
dbSNP: rs6894249
rs6894249
0.776 0.160 5 132461855 non coding transcript exon variant A/G snv 0.45
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2018 2018
dbSNP: rs6894249
rs6894249
0.776 0.160 5 132461855 non coding transcript exon variant A/G snv 0.45
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs3749833
rs3749833
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 2 2019 2019
dbSNP: rs10076733
rs10076733
1.000 0.040 5 132425039 intron variant G/T snv 0.17
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.700 1.000 1 2019 2019
dbSNP: rs1023518
rs1023518
1.000 0.080 5 132458080 intron variant G/T snv 0.26
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs10900807
rs10900807
5 132421788 intron variant G/C snv 0.20
CUI: C0523677
Disease: Glycine measurement
Glycine measurement
0.700 1.000 1 2019 2019
dbSNP: rs12515180
rs12515180
5 132449992 intron variant C/T snv 0.28
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs17622378
rs17622378
0.790 0.200 5 132442760 intron variant A/G snv 0.28
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma
0.700 1.000 1 2019 2019
dbSNP: rs17622378
rs17622378
0.790 0.200 5 132442760 intron variant A/G snv 0.28
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs3749833
rs3749833
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23
CUI: C0035242
Disease: Respiratory Tract Diseases
Respiratory Tract Diseases
0.700 1.000 1 2019 2019
dbSNP: rs3749833
rs3749833
0.925 0.080 5 132463934 non coding transcript exon variant T/C snv 0.23
CUI: C0264408
Disease: Childhood asthma
Childhood asthma
0.700 1.000 1 2019 2019
dbSNP: rs6866614
rs6866614
0.925 0.080 5 132451445 intron variant A/G snv 0.71
CUI: C0004096
Disease: Asthma
Asthma
0.700 1.000 1 2019 2019
dbSNP: rs6866614
rs6866614
0.925 0.080 5 132451445 intron variant A/G snv 0.71
CUI: C0741260
Disease: Adult onset asthma
Adult onset asthma
0.700 1.000 1 2019 2019
dbSNP: rs6867325
rs6867325
5 132448313 intron variant A/G;T snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs6894249
rs6894249
0.776 0.160 5 132461855 non coding transcript exon variant A/G snv 0.45
CUI: C0013595
Disease: Eczema
Eczema
0.700 1.000 1 2019 2019
dbSNP: rs7719499
rs7719499
5 132478399 intron variant C/G snv 0.37
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.700 1.000 1 2019 2019