rs17563161, SLC9A3

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.
Exocrine pancreatic insufficiency
CUI: C0267963
Disease: Exocrine pancreatic insufficiency
26 0.882 0.040 5 497509 intron variant G/A snv 0.18 0.010 1.000 1 2018 2018
Lung diseases
CUI: C0024115
Disease: Lung diseases
50 0.882 0.040 5 497509 intron variant G/A snv 0.18 0.010 1.000 1 2014 2014
Meconium ileus
CUI: C2939175
Disease: Meconium ileus
16 0.882 0.040 5 497509 intron variant G/A snv 0.18 0.010 1.000 1 2014 2014
Pancreatic Insufficiency
CUI: C0030293
Disease: Pancreatic Insufficiency
23 0.882 0.040 5 497509 intron variant G/A snv 0.18 0.010 1.000 1 2018 2018