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: rs72554665
rs72554665
1.000 0.120 X 154532269 missense variant C/A;G;T snv 8.1E-04; 1.1E-05; 1.1E-05
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 1.000 40 1984 2019
dbSNP: rs78365220
rs78365220
1.000 0.120 X 154535270 missense variant A/C;G snv 5.5E-06; 5.5E-06 9.5E-06
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 1.000 27 1988 2019
dbSNP: rs76645461
rs76645461
1.000 0.120 X 154536156 missense variant A/G snv 1.1E-05
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 1.000 22 1988 2019
dbSNP: rs78478128
rs78478128
0.851 0.160 X 154536168 missense variant G/C snv 1.7E-04 1.1E-04
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 1.000 21 1988 2019
dbSNP: rs137852327
rs137852327
0.882 0.120 X 154533122 missense variant C/T snv 2.2E-04 9.4E-05
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 1.000 15 1988 2016
dbSNP: rs5030869
rs5030869
0.882 0.120 X 154532990 missense variant C/A;T snv 5.5E-06; 1.9E-04 6.6E-05
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 1.000 11 1988 2015
dbSNP: rs137852314
rs137852314
0.851 0.120 X 154534495 missense variant C/T snv 4.4E-05 5.7E-05
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 1.000 10 1989 2016
dbSNP: rs5030868
rs5030868
0.827 0.160 X 154534419 missense variant G/A snv 2.6E-03 4.8E-04
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 1.000 10 1988 2014
dbSNP: rs76723693
rs76723693
0.882 0.160 X 154533025 missense variant A/G snv 5.3E-04 1.5E-03
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 1.000 8 1988 2017
dbSNP: rs398123546
rs398123546
0.925 0.120 X 154532390 missense variant G/A snv 1.5E-04 1.5E-04
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 1.000 7 1993 2015
dbSNP: rs137852318
rs137852318
0.925 0.120 X 154533596 missense variant C/A;G;T snv 7.0E-04
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 1.000 6 1969 1996
dbSNP: rs137852340
rs137852340
1.000 0.120 X 154546061 missense variant T/C snv 1.5E-04 7.6E-05
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 1.000 5 1999 2018
dbSNP: rs137852331
rs137852331
1.000 0.120 X 154534489 missense variant T/C snv 4.9E-05 3.8E-05
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 1.000 4 1992 2008
dbSNP: rs137852316
rs137852316
0.925 0.120 X 154532676 missense variant C/T snv
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 0
dbSNP: rs137852317
rs137852317
1.000 0.120 X 154532411 missense variant C/T snv
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 0
dbSNP: rs137852326
rs137852326
1.000 0.120 X 154534345 missense variant C/A;G snv 5.5E-06
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 0
dbSNP: rs137852329
rs137852329
1.000 0.120 X 154532765 missense variant G/T snv
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 0
dbSNP: rs137852332
rs137852332
1.000 0.120 X 154534389 missense variant C/G;T snv
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 0
dbSNP: rs137852334
rs137852334
0.925 0.120 X 154532695 missense variant G/A snv
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 0
dbSNP: rs137852335
rs137852335
0.925 0.120 X 154532674 missense variant C/G snv
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 0
dbSNP: rs137852336
rs137852336
1.000 0.120 X 154532625 missense variant C/T snv
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 0
dbSNP: rs137852337
rs137852337
1.000 0.120 X 154532434 missense variant C/G;T snv
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 0
dbSNP: rs137852339
rs137852339
1.000 0.120 X 154533044 missense variant C/T snv 1.2E-03 1.8E-04
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 0
dbSNP: rs5030872
rs5030872
0.882 0.160 X 154534440 missense variant T/A snv 1.4E-04 4.7E-04
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.800 0
dbSNP: rs138687036
rs138687036
1.000 0.120 X 154535963 missense variant G/A snv 2.2E-05 6.6E-05
ANEMIA, NONSPHEROCYTIC HEMOLYTIC, DUE TO G6PD DEFICIENCY
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases 0.700 1.000 19 1988 2019