Source: ALL
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: rs1553853557
rs1553853557 		0.882 0.040 3 184346710 missense variant T/G snv
CUI: C1854107
Disease: Hyperaldosteronism, Familial, Type II
Hyperaldosteronism, Familial, Type II 		Endocrine System Diseases 0.800 1.000 2 2018 2018
dbSNP: rs1553853557
rs1553853557 		0.882 0.040 3 184346710 missense variant T/G snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.700 0
dbSNP: rs1553853557
rs1553853557 		0.882 0.040 3 184346710 missense variant T/G snv
CUI: C4023208
Disease: Glucocortocoid-insensitive primary hyperaldosteronism
Glucocortocoid-insensitive primary hyperaldosteronism 		Endocrine System Diseases 0.700 0
dbSNP: rs1553853557
rs1553853557 		0.882 0.040 3 184346710 missense variant T/G snv
CUI: C1384514
Disease: Conn Syndrome
Conn Syndrome 		Endocrine System Diseases 0.700 0