Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1050828
rs1050828
0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02
Deficiency of glucose-6-phosphate dehydrogenase
0.080 0.875 8 1992 2014
dbSNP: rs137852316
rs137852316
0.925 0.120 X 154532676 missense variant C/T snv
Chronic non-spherocytic hemolytic anemia
0.010 1.000 1 1992 1992
dbSNP: rs398123546
rs398123546
0.925 0.120 X 154532390 missense variant G/A snv 1.5E-04 1.5E-04
Deficiency of glucose-6-phosphate dehydrogenase
0.020 1.000 2 1993 2013
dbSNP: rs137852320
rs137852320
0.925 0.120 X 154532698 missense variant T/C snv
Chronic non-spherocytic hemolytic anemia
0.010 < 0.001 1 1994 1994
dbSNP: rs5030868
rs5030868
0.827 0.160 X 154534419 missense variant G/A snv 2.6E-03 4.8E-04
Deficiency of glucose-6-phosphate dehydrogenase
0.720 1.000 2 1995 2014
dbSNP: rs78478128
rs78478128
0.851 0.160 X 154536168 missense variant G/C snv 1.7E-04 1.1E-04
Deficiency of glucose-6-phosphate dehydrogenase
0.010 1.000 1 1995 1995
dbSNP: rs5030872
rs5030872
0.882 0.160 X 154534440 missense variant T/A snv 1.4E-04 4.7E-04
CUI: C0015702
Disease: Favism
Favism
0.010 1.000 1 1996 1996
dbSNP: rs137852334
rs137852334
0.925 0.120 X 154532695 missense variant G/A snv
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder)
0.010 1.000 1 2002 2002
dbSNP: rs200111236
rs200111236
0.882 0.200 X 154534463 missense variant G/A;C snv 2.8E-04; 5.5E-06
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
0.010 1.000 1 2002 2002
dbSNP: rs200111236
rs200111236
0.882 0.200 X 154534463 missense variant G/A;C snv 2.8E-04; 5.5E-06
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2002 2002
dbSNP: rs200111236
rs200111236
0.882 0.200 X 154534463 missense variant G/A;C snv 2.8E-04; 5.5E-06
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2002 2002
dbSNP: rs200111236
rs200111236
0.882 0.200 X 154534463 missense variant G/A;C snv 2.8E-04; 5.5E-06
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2002 2002
dbSNP: rs200111236
rs200111236
0.882 0.200 X 154534463 missense variant G/A;C snv 2.8E-04; 5.5E-06
CUI: C0015702
Disease: Favism
Favism
0.010 1.000 1 2002 2002
dbSNP: rs387906470
rs387906470
1.000 0.080 X 154532785 missense variant G/A snv
CUI: C0017551
Disease: Gilbert Disease (disorder)
Gilbert Disease (disorder)
0.010 1.000 1 2002 2002
dbSNP: rs78478128
rs78478128
0.851 0.160 X 154536168 missense variant G/C snv 1.7E-04 1.1E-04
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 1.000 1 2002 2002
dbSNP: rs78478128
rs78478128
0.851 0.160 X 154536168 missense variant G/C snv 1.7E-04 1.1E-04
CUI: C0002878
Disease: Anemia, Hemolytic
Anemia, Hemolytic
0.010 1.000 1 2002 2002
dbSNP: rs78478128
rs78478128
0.851 0.160 X 154536168 missense variant G/C snv 1.7E-04 1.1E-04
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.010 1.000 1 2002 2002
dbSNP: rs78478128
rs78478128
0.851 0.160 X 154536168 missense variant G/C snv 1.7E-04 1.1E-04
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.010 1.000 1 2002 2002
dbSNP: rs78478128
rs78478128
0.851 0.160 X 154536168 missense variant G/C snv 1.7E-04 1.1E-04
CUI: C0015702
Disease: Favism
Favism
0.010 1.000 1 2002 2002
dbSNP: rs1050829
rs1050829
0.827 0.160 X 154535277 missense variant T/A;C snv 1.7E-04; 2.6E-02
Deficiency of glucose-6-phosphate dehydrogenase
0.060 0.833 6 2005 2019
dbSNP: rs2230037
rs2230037
0.925 0.160 X 154532439 synonymous variant A/G snv
Deficiency of glucose-6-phosphate dehydrogenase
0.020 1.000 2 2008 2017
dbSNP: rs370451233
rs370451233
1.000 0.040 X 154535315 missense variant T/C snv 1.1E-05 1.9E-05
CUI: C0272087
Disease: Congenital Methemoglobinemia
Congenital Methemoglobinemia
0.010 1.000 1 2008 2008
dbSNP: rs5030868
rs5030868
0.827 0.160 X 154534419 missense variant G/A snv 2.6E-03 4.8E-04
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 1.000 1 2009 2009
dbSNP: rs5030868
rs5030868
0.827 0.160 X 154534419 missense variant G/A snv 2.6E-03 4.8E-04
CUI: C0037054
Disease: Sickle Cell Trait
Sickle Cell Trait
0.010 1.000 1 2009 2009
dbSNP: rs370918918
rs370918918
1.000 0.120 X 154535176 missense variant C/G snv 9.7E-04 8.5E-05
Deficiency of glucose-6-phosphate dehydrogenase
0.010 1.000 1 2010 2010