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: rs374270497
rs374270497
0.925 0.040 6 131860504 missense variant C/A;T snv 2.0E-05
CUI: C1859727
Disease: Arterial calcification of infancy
Arterial calcification of infancy
Nutritional and Metabolic Diseases 0.700 1.000 1 2008 2008
dbSNP: rs1243920034
rs1243920034
0.925 0.040 6 131873023 missense variant A/G snv
CUI: C1859727
Disease: Arterial calcification of infancy
Arterial calcification of infancy
Nutritional and Metabolic Diseases 0.010 1.000 1 2012 2012