DLD, dihydrolipoamide dehydrogenase, 1738

N. diseases: 190; N. variants: 42
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: rs121964987
rs121964987
1.000 0.040 7 107902340 missense variant A/G snv
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.800 1.000 12 1993 2009
dbSNP: rs121964989
rs121964989
1.000 0.040 7 107919212 missense variant A/G snv
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.800 1.000 12 1993 2009
dbSNP: rs121964991
rs121964991
1.000 0.040 7 107917404 missense variant T/C snv
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.800 1.000 12 1993 2009
dbSNP: rs397514649
rs397514649
1.000 0.040 7 107919071 missense variant A/T snv
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.810 1.000 12 1993 2009
dbSNP: rs397514650
rs397514650
1.000 0.040 7 107919079 missense variant A/G snv
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.800 1.000 12 1993 2009
dbSNP: rs397514651
rs397514651
1.000 0.040 7 107901759 missense variant T/C snv
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.800 1.000 12 1993 2009
dbSNP: rs1328820332
rs1328820332
1.000 0.040 7 107915697 splice donor variant G/A snv 7.0E-06
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 1.000 2 1996 1999
dbSNP: rs1554400699
rs1554400699
1.000 0.040 7 107919055 frameshift variant G/- delins
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 1.000 2 1992 1995
dbSNP: rs1554400704
rs1554400704
1.000 0.040 7 107919064 frameshift variant TGTG/- del
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 1.000 2 1992 1995
dbSNP: rs1554400713
rs1554400713
1.000 0.040 7 107919079 frameshift variant AG/- delins
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 1.000 2 1992 1995
dbSNP: rs1383147053
rs1383147053
0.882 0.120 7 107901762 missense variant G/A snv
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon
Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1383147053
rs1383147053
0.882 0.120 7 107901762 missense variant G/A snv
CUI: C0027651
Disease: Neoplasms
Neoplasms
Neoplasms 0.010 1.000 1 2005 2005
dbSNP: rs1383147053
rs1383147053
0.882 0.120 7 107901762 missense variant G/A snv
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia
Nutritional and Metabolic Diseases 0.010 1.000 1 2005 2005
dbSNP: rs1383147053
rs1383147053
0.882 0.120 7 107901762 missense variant G/A snv
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma
Digestive System Diseases; Neoplasms 0.010 1.000 1 2018 2018
dbSNP: rs1554396895
rs1554396895
1.000 0.040 7 107893265 frameshift variant C/- del
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 1.000 1 1999 1999
dbSNP: rs1554396908
rs1554396908
1.000 0.040 7 107893279 splice donor variant G/T snv
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 1.000 1 2014 2014
dbSNP: rs1040811473
rs1040811473
1.000 0.040 7 107906311 frameshift variant A/-;AA delins
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs1057516698
rs1057516698
1.000 0.040 7 107893272 stop gained C/T snv
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs1057517214
rs1057517214
1.000 0.040 7 107902346 frameshift variant -/A delins
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs111257462
rs111257462
1.000 0.040 7 107891290 splice donor variant G/A;C snv
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs1554398193
rs1554398193
1.000 0.040 7 107901818 splice donor variant G/A snv
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs1554398264
rs1554398264
1.000 0.040 7 107902324 splice acceptor variant G/A snv
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs1554398461
rs1554398461
1.000 0.040 7 107903476 splice acceptor variant A/G snv
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs1554398624
rs1554398624
1.000 0.040 7 107904956 splice acceptor variant AG/T delins
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs1554398625
rs1554398625
1.000 0.040 7 107904964 frameshift variant A/- delins
NADH cytochrome B5 reductase deficiency
Hemic and Lymphatic Diseases 0.700 0