Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs737337
rs737337
0.925 0.040 19 11236817 synonymous variant T/C snv 0.15 0.20
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2010 2013
dbSNP: rs12979813
rs12979813
19 11232027 intron variant A/G snv 0.30
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2013 2013
dbSNP: rs2278426
rs2278426
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2013 2013