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: rs1131692061
rs1131692061
MT 12271 non coding transcript exon variant T/C snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
Nutritional and Metabolic Diseases 0.700 0
dbSNP: rs1131692062
rs1131692062
MT 12283 non coding transcript exon variant G/A snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
Nutritional and Metabolic Diseases 0.700 0
dbSNP: rs1131692063
rs1131692063
1.000 0.160 MT 13051 missense variant G/A snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
Nutritional and Metabolic Diseases 0.700 0
dbSNP: rs267606897
rs267606897
0.882 0.200 MT 13513 missense variant G/A snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
Nutritional and Metabolic Diseases 0.700 0
dbSNP: rs2853493
rs2853493
MT 11467 synonymous variant A/G snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
Nutritional and Metabolic Diseases 0.700 0
dbSNP: rs2853499
rs2853499
MT 12372 synonymous variant G/A snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
Nutritional and Metabolic Diseases 0.700 0