Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2823819
rs2823819
MIR99AHG
1.000 0.040 21 16455971 intron variant A/G snv 0.22
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.800 1.000 1 2010 2010
dbSNP: rs11088565
rs11088565
MIR99AHG
21 16101911 intron variant C/G;T snv
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs11909251
rs11909251
MIR99AHG
21 16110067 intron variant G/T snv 0.33
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs2823612
rs2823612
MIR99AHG
21 16107233 intron variant T/C snv 0.32
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs2823615
rs2823615
MIR99AHG
21 16110813 intron variant A/T snv 0.33
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs9975788
rs9975788
MIR99AHG
21 16092495 intron variant C/T snv 0.32
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs9983980
rs9983980
MIR99AHG
21 16100046 intron variant C/T snv 0.32
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012