rs6486121, ARNTL

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.
High density lipoprotein measurement
1440 11 13334223 intron variant C/T snv 0.53 0.700 1.000 1 2018 2018
Serum transferrin measurement
CUI: C0428545
Disease: Serum transferrin measurement
10 11 13334223 intron variant C/T snv 0.53 0.700 1.000 1 2014 2014
Transferrin measurement
CUI: C0202105
Disease: Transferrin measurement
10 11 13334223 intron variant C/T snv 0.53 0.700 1.000 1 2014 2014