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: rs137854499
rs137854499
1.000 0.080 9 104788469 missense variant A/G snv
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.700 1.000 8 1999 2013
dbSNP: rs28933692
rs28933692
1.000 0.080 9 104818830 missense variant C/A;T snv 8.0E-06
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.700 1.000 8 1999 2013
dbSNP: rs145183203
rs145183203
1.000 0.080 9 104884475 missense variant G/A snv 1.4E-03 1.2E-03
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.700 1.000 7 1999 2013
dbSNP: rs760768125
rs760768125
1.000 0.080 9 104792854 missense variant G/A snv 2.4E-05 2.8E-05
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.700 1.000 7 1999 2013
dbSNP: rs760507032
rs760507032
1.000 0.080 9 104796354 missense variant G/C snv 2.8E-05 1.4E-05
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.700 1.000 5 2001 2012
dbSNP: rs369098049
rs369098049
1.000 0.080 9 104785592 missense variant G/A snv 4.4E-05 9.1E-05
CUI: C1704429
Disease: Hypoalphalipoproteinemia, Familial
Hypoalphalipoproteinemia, Familial
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases 0.700 0