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: rs12507197
rs12507197
4 38662039 intron variant T/C snv 0.18
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement
0.700 1.000 1 2019 2019
dbSNP: rs337606
rs337606
4 38657642 intron variant G/A;C;T snv
CUI: C0005890
Disease: Body Height
Body Height
0.700 1.000 1 2019 2019
dbSNP: rs337638
rs337638
1.000 0.040 4 38603186 intron variant T/C snv 0.30
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute
0.700 1.000 1 2017 2017
dbSNP: rs4833079
rs4833079
1.000 0.040 4 38653060 intron variant T/C snv 0.30
CUI: C1305855
Disease: Body mass index
Body mass index
0.700 1.000 1 2018 2018
dbSNP: rs6855993
rs6855993
4 38607291 intron variant A/T snv 0.27
Finding of Mean Corpuscular Hemoglobin
0.700 1.000 1 2016 2016
dbSNP: rs73232881
rs73232881
4 38662510 intron variant T/C snv 0.17
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2019 2019
dbSNP: rs75504410
rs75504410
4 38656198 intron variant G/A snv 6.6E-02
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.700 1.000 1 2016 2016
dbSNP: rs75504410
rs75504410
4 38656198 intron variant G/A snv 6.6E-02
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.700 1.000 1 2016 2016