Source: GWASCAT

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: rs2294915
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2018 2018
dbSNP: rs2294915
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		0.700 1.000 1 2016 2016
dbSNP: rs2294915
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		0.700 1.000 1 2019 2019
dbSNP: rs2294915
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv
CUI: C1883008
Disease: Serum Alanine Aminotransferase Measurement
Serum Alanine Aminotransferase Measurement 		0.700 1.000 1 2019 2019
dbSNP: rs2294915
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv
CUI: C0201836
Disease: Alanine aminotransferase measurement
Alanine aminotransferase measurement 		0.700 1.000 1 2019 2019