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: rs1861525
rs1861525 		1.000 0.080 7 25121983 3 prime UTR variant A/G snv 3.2E-02
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		Nervous System Diseases; Mental Disorders 0.800 1.000 1 2014 2014
dbSNP: rs121918552
rs121918552 		1.000 0.040 7 25123996 missense variant C/T snv
CUI: C0040034
Disease: Thrombocytopenia
Thrombocytopenia 		Hemic and Lymphatic Diseases 0.710 1.000 2 2014 2019
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