rs9302635, DHX38

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.
Blood Protein Measurement
CUI: C2985280
Disease: Blood Protein Measurement
2575 16 72110275 intron variant T/C;G snv 0.700 1.000 1 2018 2018
Ferritin measurement
CUI: C0373607
Disease: Ferritin measurement
21 16 72110275 intron variant T/C;G snv 0.700 1.000 1 2017 2017
Serum ferritin measurement
CUI: C0696113
Disease: Serum ferritin measurement
21 16 72110275 intron variant T/C;G snv 0.700 1.000 1 2017 2017
Uric acid measurement (procedure)
CUI: C0202239
Disease: Uric acid measurement (procedure)
1463 16 72110275 intron variant T/C;G snv 0.700 1.000 1 2019 2019