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: rs17824620
rs17824620
RPH3A
12 112663189 intron variant C/A snv 0.26
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.800 1.000 1 2011 2011
dbSNP: rs233716
rs233716
RPH3A
1.000 0.080 12 112602139 intron variant C/T snv 0.58
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.700 1.000 1 2013 2013
dbSNP: rs233722
rs233722
RPH3A
1.000 0.080 12 112593670 intron variant G/A snv 0.53
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		0.700 1.000 1 2013 2013
dbSNP: rs2891403
rs2891403
RPH3A
1.000 0.040 12 112699767 intron variant A/G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		0.700 1.000 1 2013 2013
dbSNP: rs886476
rs886476
RPH3A
1.000 0.040 12 112881666 intron variant G/A snv 0.49
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2012 2012