rs11689538, TFCP2L1

N. diseases: 3
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.
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 2 121238062 intron variant G/C snv 0.11 0.700 1.000 1 2016 2016
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 2 121238062 intron variant G/C snv 0.11 0.700 1.000 1 2016 2016
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 2 121238062 intron variant G/C snv 0.11 0.700 1.000 1 2016 2016