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: rs9523762
rs9523762
GPC5 ; LOC105370315
0.925 0.120 13 92679633 intron variant G/A snv 0.39
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.820 1.000 1 2009 2013
dbSNP: rs7982677
rs7982677
GPC5
1.000 0.080 13 92336070 intron variant C/A snv 0.29
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.800 1.000 1 2013 2013
dbSNP: rs1411741
rs1411741
GPC5
1.000 0.080 13 92101599 intron variant A/G snv 0.98
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009
dbSNP: rs17267292
rs17267292
GPC5 ; LOC105370315
13 92670893 intron variant T/C snv 0.22
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2008 2008
dbSNP: rs4771856
rs4771856
GPC5 ; GPC5-AS2
1.000 0.080 13 92342256 intron variant C/A snv 0.29
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.700 1.000 1 2013 2013
dbSNP: rs7328464
rs7328464
GPC5
13 91849410 intron variant C/T snv 0.14
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs7981515
rs7981515
GPC5
13 91870760 intron variant G/T snv 0.13
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012