rs9376090, HBS1L

N. diseases: 7
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.
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 6 135090090 intron variant T/C snv 0.19 0.800 1.000 3 2013 2018
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 6 135090090 intron variant T/C snv 0.19 0.800 1.000 2 2012 2017
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 6 135090090 intron variant T/C snv 0.19 0.800 1.000 2 2009 2018
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 6 135090090 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 6 135090090 intron variant T/C snv 0.19 0.700 1.000 1 2016 2016
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 6 135090090 intron variant T/C snv 0.19 0.700 1.000 1 2018 2018
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 6 135090090 intron variant T/C snv 0.19 0.700 1.000 1 2017 2017