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: rs7130284
rs7130284
NOX4
11 89415204 intron variant C/T snv 0.11
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		0.800 1.000 1 2013 2013
dbSNP: rs957140
rs957140
NOX4
11 89468459 intron variant G/A snv 0.40
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement 		0.800 1.000 1 2013 2013
dbSNP: rs11018644
rs11018644
NOX4
11 89528362 intergenic variant G/T snv 7.6E-02
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs1847138
rs1847138
NOX4
1.000 0.080 11 89361438 intron variant T/C snv 5.2E-03
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		0.700 1.000 1 2009 2009