rs7775698, HBS1L

N. diseases: 8
Source: GWASDB ×
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.
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
87 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 3 2009 2013
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4267 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 2 2010 2012
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
70 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 2 2009 2013
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
480 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 2 2009 2012
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
9 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 1 2010 2012
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
265 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.700 1.000 1 2011 2011
Mean corpuscular hemoglobin concentration determination
CUI: C0474535
Disease: Mean corpuscular hemoglobin concentration determination
19 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.700 1.000 1 2012 2012
Platelet mean volume determination (procedure)
CUI: C0200665
Disease: Platelet mean volume determination (procedure)
77 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.700 1.000 1 2012 2012