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: rs17309827
rs17309827
SLC22A23
1.000 0.040 6 3433084 intron variant T/G snv 0.30
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 2 2008 2010
dbSNP: rs9378357
rs9378357
SLC22A23 ; PSMG4
6 3294590 intron variant G/T snv 0.20
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012