rs1331309, HBS1L

N. diseases: 2
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 6 135085040 intron variant T/G snv 0.19 0.700 1.000 1 2017 2017
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 6 135085040 intron variant T/G snv 0.19 0.700 1.000 1 2018 2018