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: rs6589565
rs6589565
BUD13
11 116769521 intron variant A/G snv 0.93
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs7930786
rs7930786
BUD13
11 116754011 intron variant C/G snv 0.92
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012
dbSNP: rs28927680
rs28927680
BUD13
11 116748357 3 prime UTR variant C/G;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 3 2008 2019
dbSNP: rs28927680
rs28927680
BUD13
11 116748357 3 prime UTR variant C/G;T snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 2 2012 2019
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