CYCS, cytochrome c, somatic, 54205

N. diseases: 67; N. variants: 4
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121918552
rs121918552
1.000 0.040 7 25123996 missense variant C/T snv
CUI: C2677608
Disease: Thrombocytopenia 4
Thrombocytopenia 4
Hemic and Lymphatic Diseases 0.810 1.000 2 2008 2014
dbSNP: rs1562515878
rs1562515878
1.000 0.040 7 25123716 inframe deletion TTT/- delins
CUI: C2677608
Disease: Thrombocytopenia 4
Thrombocytopenia 4
Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs886037737
rs886037737
1.000 0.040 7 25123975 missense variant A/G snv
CUI: C2677608
Disease: Thrombocytopenia 4
Thrombocytopenia 4
Hemic and Lymphatic Diseases 0.700 0