rs7085433, TIMM23

N. diseases: 4
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.
Finding of Mean Corpuscular Hemoglobin
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
1206 1.000 0.040 10 46002468 intron variant C/T snv 9.5E-02 0.700 1.000 2 2010 2017
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 1.000 0.040 10 46002468 intron variant C/T snv 9.5E-02 0.700 1.000 1 2019 2019
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 1.000 0.040 10 46002468 intron variant C/T snv 9.5E-02 0.700 1.000 1 2010 2010
Mean Corpuscular Volume (result)
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
549 1.000 0.040 10 46002468 intron variant C/T snv 9.5E-02 0.700 1.000 1 2010 2010