rs4954218, MAP3K19

N. diseases: 5
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.
Keratoconus
CUI: C0022578
Disease: Keratoconus
83 0.925 0.080 2 135045855 intron variant G/T snv 0.83 0.740 1.000 4 2012 2017
Corneal Topography
CUI: C0524957
Disease: Corneal Topography
98 0.925 0.080 2 135045855 intron variant G/T snv 0.83 0.700 1.000 1 2012 2012
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.925 0.080 2 135045855 intron variant G/T snv 0.83 0.700 1.000 1 2017 2017
Congenital Abnormality
CUI: C0000768
Disease: Congenital Abnormality
73 0.925 0.080 2 135045855 intron variant G/T snv 0.83 0.010 1.000 1 2012 2012
Deformity
CUI: C0302142
Disease: Deformity
26 0.925 0.080 2 135045855 intron variant G/T snv 0.83 0.010 1.000 1 2012 2012