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: rs8037818
rs8037818 		15 32635275 intron variant C/T snv 0.79
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.800 1.000 1 2012 2012
dbSNP: rs11632524
rs11632524 		15 32633875 intron variant C/T snv 0.70
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs11634439
rs11634439 		15 32630746 intron variant T/G snv 0.74
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs28670903
rs28670903 		15 32640104 intron variant G/T snv
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012