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: rs137853103
rs137853103
1.000 0.040 4 108033239 missense variant C/T snv
Hyperinsulinemic Hypoglycemia, Familial, 4
Nutritional and Metabolic Diseases 0.800 1.000 1 2001 2001
dbSNP: rs375717077
rs375717077
1.000 0.040 4 108027757 stop gained C/T snv 1.2E-05 1.4E-05
Hyperinsulinemic Hypoglycemia, Familial, 4
Nutritional and Metabolic Diseases 0.700 0
dbSNP: rs786200932
rs786200932
1.000 0.040 4 108024034 3 prime UTR variant G/A;T snv
Hyperinsulinemic Hypoglycemia, Familial, 4
Nutritional and Metabolic Diseases 0.700 0