rs35188965, SLC12A7

N. diseases: 12
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
RDW - Red blood cell distribution width result
988 5 1104823 intron variant C/G;T snv 0.700 1.000 3 2016 2019
Red cell distribution width determination
988 5 1104823 intron variant C/G;T snv 0.700 1.000 3 2016 2019
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 5 1104823 intron variant C/G;T snv 0.700 1.000 2 2016 2019
Blood basophil count (lab test)
CUI: C0200641
Disease: Blood basophil count (lab test)
452 5 1104823 intron variant C/G;T snv 0.700 1.000 1 2016 2016
Eosinophil count procedure
CUI: C0200638
Disease: Eosinophil count procedure
1144 5 1104823 intron variant C/G;T snv 0.700 1.000 1 2016 2016
Finding of Mean Corpuscular Hemoglobin
1206 5 1104823 intron variant C/G;T snv 0.700 1.000 1 2019 2019
Granulocyte count
CUI: C0857490
Disease: Granulocyte count
150 5 1104823 intron variant C/G;T snv 0.700 1.000 1 2016 2016
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 5 1104823 intron variant C/G;T snv 0.700 1.000 1 2016 2016
Neutrophil count (procedure)
CUI: C0200633
Disease: Neutrophil count (procedure)
234 5 1104823 intron variant C/G;T snv 0.700 1.000 1 2016 2016
Platelet Component Distribution Width Measurement
200 5 1104823 intron variant C/G;T snv 0.700 1.000 1 2016 2016
Platelet mean volume determination (procedure)
371 5 1104823 intron variant C/G;T snv 0.700 1.000 1 2016 2016
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 5 1104823 intron variant C/G;T snv 0.700 1.000 1 2019 2019