rs587777042, CYC1

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.
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6
CUI: C3809553
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6
2 0.882 0.040 8 144096615 missense variant C/T snv 4.0E-06 0.800 1.000 1 2013 2013
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.882 0.040 8 144096615 missense variant C/T snv 4.0E-06 0.010 1.000 1 2013 2013
Ketosis
CUI: C0022638
Disease: Ketosis
11 0.882 0.040 8 144096615 missense variant C/T snv 4.0E-06 0.010 1.000 1 2013 2013