rs217181, TXNL4B

N. diseases: 6
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 72080103 intron variant C/T snv 0.20 0.700 1.000 1 2018 2018
Calcification of coronary artery
CUI: C1611184
Disease: Calcification of coronary artery
205 16 72080103 intron variant C/T snv 0.20 0.700 1.000 1 2012 2012
Ferritin measurement
CUI: C0373607
Disease: Ferritin measurement
21 16 72080103 intron variant C/T snv 0.20 0.700 1.000 1 2017 2017
Serum albumin measurement
CUI: C0523465
Disease: Serum albumin measurement
3282 16 72080103 intron variant C/T snv 0.20 0.700 1.000 1 2012 2012
Serum ferritin measurement
CUI: C0696113
Disease: Serum ferritin measurement
21 16 72080103 intron variant C/T snv 0.20 0.700 1.000 1 2017 2017
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 16 72080103 intron variant C/T snv 0.20 0.700 1.000 1 2012 2012