rs7776054, HBS1L

N. diseases: 13
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.
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 6 135097778 intron variant A/G snv 0.24 0.800 1.000 4 2012 2018
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
1206 6 135097778 intron variant A/G snv 0.24 0.800 1.000 3 2009 2018
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 6 135097778 intron variant A/G snv 0.24 0.700 1.000 2 2016 2017
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 6 135097778 intron variant A/G snv 0.24 0.700 1.000 1 2017 2017
Hemoglobin A2 measurement
CUI: C0474543
Disease: Hemoglobin A2 measurement
5 6 135097778 intron variant A/G snv 0.24 0.700 1.000 1 2015 2015
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 6 135097778 intron variant A/G snv 0.24 0.700 1.000 1 2015 2015
Low density lipoprotein cholesterol measurement
CUI: C0202117
Disease: Low density lipoprotein cholesterol measurement
1142 6 135097778 intron variant A/G snv 0.24 0.700 1.000 1 2017 2017
Monocyte count procedure
CUI: C0200637
Disease: Monocyte count procedure
296 6 135097778 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016
Monocyte count result
CUI: C0750880
Disease: Monocyte count result
296 6 135097778 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016
Platelet Count measurement
CUI: C0032181
Disease: Platelet Count measurement
457 6 135097778 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016
RDW - Red blood cell distribution width result
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
988 6 135097778 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 6 135097778 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016
Red cell distribution width determination
CUI: C0427460
Disease: Red cell distribution width determination
988 6 135097778 intron variant A/G snv 0.24 0.700 1.000 1 2016 2016