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: rs7998875
rs7998875
13 110289053 intron variant G/A;T snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs7998875
rs7998875
13 110289053 intron variant G/A;T snv
High density lipoprotein measurement
0.700 1.000 1 2012 2012
dbSNP: rs7998875
rs7998875
13 110289053 intron variant G/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012