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: rs4846914
rs4846914
GALNT2
0.925 0.080 1 230159944 intron variant G/A snv 0.45
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 4 2008 2019
dbSNP: rs2144300
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 2 2008 2018
dbSNP: rs17315646
rs17315646
GALNT2
1 230159560 intron variant C/A;G snv 0.45
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2281719
rs2281719
GALNT2
1.000 0.040 1 230161913 intron variant C/T snv 0.45
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs2296065
rs2296065
GALNT2
1 230166030 intron variant G/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs4846918
rs4846918
GALNT2
1 230164840 intron variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012
dbSNP: rs611841
rs611841
GALNT2
1 230173735 intron variant C/A;G snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012