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: rs12734338
rs12734338
PPP1R12B
0.925 0.120 1 202500595 intron variant T/C snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.800 1.000 1 2013 2013
dbSNP: rs12734338
rs12734338
PPP1R12B
0.925 0.120 1 202500595 intron variant T/C snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.800 1.000 1 2013 2013
dbSNP: rs12734001
rs12734001
PPP1R12B
1.000 0.080 1 202421786 intron variant C/T snv 3.5E-05
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011
dbSNP: rs12734001
rs12734001
PPP1R12B
1.000 0.080 1 202421786 intron variant C/T snv 3.5E-05
CUI: C0162534
Disease: Prion Diseases
Prion Diseases 		0.700 1.000 1 2012 2012
dbSNP: rs12739262
rs12739262
PPP1R12B
1 202422615 splice region variant C/T snv 1.5E-04 7.0E-05
CUI: C0162701
Disease: Polysomnography
Polysomnography 		0.700 1.000 1 2012 2012
dbSNP: rs3817222
rs3817222
PPP1R12B
1.000 0.080 1 202495632 missense variant C/T snv 3.6E-05 7.0E-06
CUI: C0004096
Disease: Asthma
Asthma 		0.700 1.000 1 2011 2011