rs1553787823, MYLK

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.
Abnormality of the bladder
CUI: C0149632
Disease: Abnormality of the bladder
2 0.882 0.120 3 123664245 frameshift variant -/GCTTTCC delins 0.700 1.000 1 2017 2017
Fetal megacystis
CUI: C2931117
Disease: Fetal megacystis
4 0.882 0.120 3 123664245 frameshift variant -/GCTTTCC delins 0.700 1.000 1 2017 2017
Microcolon
CUI: C0266200
Disease: Microcolon
2 0.882 0.120 3 123664245 frameshift variant -/GCTTTCC delins 0.700 1.000 1 2017 2017
Visceral Myopathy
CUI: C0042781
Disease: Visceral Myopathy
19 0.882 0.120 3 123664245 frameshift variant -/GCTTTCC delins 0.700 1.000 1 2017 2017