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: rs10097849
rs10097849
8 14672342 intron variant T/G snv 0.55
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012
dbSNP: rs10216809
rs10216809
0.925 0.080 8 14507414 intron variant C/G;T snv
CUI: C0030319
Disease: Panic Disorder
Panic Disorder
0.700 1.000 1 2009 2009
dbSNP: rs10888095
rs10888095
0.925 0.040 8 15004905 intron variant C/A;G snv
CUI: C0947622
Disease: Cholecystolithiasis
Cholecystolithiasis
0.700 1.000 1 2007 2007
dbSNP: rs10888095
rs10888095
0.925 0.040 8 15004905 intron variant C/A;G snv
CUI: C0008350
Disease: Cholelithiasis
Cholelithiasis
0.700 1.000 1 2007 2007
dbSNP: rs11203649
rs11203649
8 14659785 intron variant T/C snv 0.72
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012