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: rs151330263
rs151330263
16 252162 intron variant A/G snv 1.0E-02
CUI: C0344395
Disease: Bilirubin measurement
Bilirubin measurement
0.700 1.000 1 2019 2019
dbSNP: rs13331259
rs13331259
16 249924 intron variant A/G snv 3.0E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
16 243594 intron variant C/T snv 7.3E-03
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2019 2019
dbSNP: rs9924561
rs9924561
16 264781 intron variant G/A;T snv 2.9E-05; 6.5E-03
Corpuscular Hemoglobin Concentration Mean
0.800 1.000 3 2013 2019
dbSNP: rs13335629
rs13335629
16 260381 intron variant G/A;C snv 1.1E-02
Corpuscular Hemoglobin Concentration Mean
0.800 1.000 2 2013 2019
dbSNP: rs1122794
rs1122794
16 259156 intron variant C/A snv 0.19
Corpuscular Hemoglobin Concentration Mean
0.800 1.000 1 2012 2013
dbSNP: rs13331259
rs13331259
16 249924 intron variant A/G snv 3.0E-02
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2019 2019
dbSNP: rs13339636
rs13339636
16 248589 intron variant A/G snv 3.8E-02
Corpuscular Hemoglobin Concentration Mean
0.800 1.000 1 2013 2017
dbSNP: rs151330263
rs151330263
16 252162 intron variant A/G snv 1.0E-02
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
16 243594 intron variant C/T snv 7.3E-03
Corpuscular Hemoglobin Concentration Mean
0.700 1.000 1 2019 2019
dbSNP: rs9940149
rs9940149
1.000 0.080 16 250642 intron variant G/A snv 0.32
Diabetes Mellitus, Non-Insulin-Dependent
0.700 1.000 2 2017 2018
dbSNP: rs13331259
rs13331259
16 249924 intron variant A/G snv 3.0E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs76792961
rs76792961
16 243594 intron variant C/T snv 7.3E-03
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs1122794
rs1122794
16 259156 intron variant C/A snv 0.19
Finding of Mean Corpuscular Hemoglobin
0.800 1.000 2 2009 2017
dbSNP: rs13331259
rs13331259
16 249924 intron variant A/G snv 3.0E-02
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 2 2019 2019
dbSNP: rs9924561
rs9924561
16 264781 intron variant G/A;T snv 2.9E-05; 6.5E-03
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 2 2013 2017
dbSNP: rs13339636
rs13339636
16 248589 intron variant A/G snv 3.8E-02
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2013 2013
dbSNP: rs3743879
rs3743879
16 268475 3 prime UTR variant C/A;G snv
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2019 2019
dbSNP: rs13335629
rs13335629
16 260381 intron variant G/A;C snv 1.1E-02
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2013 2013
dbSNP: rs13339636
rs13339636
16 248589 intron variant A/G snv 3.8E-02
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
0.700 1.000 1 2017 2017
dbSNP: rs13331259
rs13331259
16 249924 intron variant A/G snv 3.0E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 2 2019 2019
dbSNP: rs9924561
rs9924561
16 264781 intron variant G/A;T snv 2.9E-05; 6.5E-03
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 2 2013 2017
dbSNP: rs13335629
rs13335629
16 260381 intron variant G/A;C snv 1.1E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2013 2013
dbSNP: rs13339636
rs13339636
16 248589 intron variant A/G snv 3.8E-02
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2017 2017
dbSNP: rs4374177
rs4374177
16 256244 intron variant A/G snv 0.25
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result)
0.700 1.000 1 2018 2018