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: rs11820589
rs11820589
BUD13
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2011 2011
dbSNP: rs11820589
rs11820589
BUD13
1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10790162
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2011 2019
dbSNP: rs10790162
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs10790162
rs10790162
BUD13
0.882 0.160 11 116768388 intron variant A/G;T snv 0.93
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2011 2011