Disease: Pseudocholinesterase Measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs11722228
SLC2A9
0.851 0.160 4 9914117 intron variant C/T snv 0.32 4
rs11754288
SLC17A4 ; SLC17A1
0.925 0.120 6 25776721 missense variant G/A snv 0.36 0.32 4
rs13129697
SLC2A9
0.925 0.120 4 9925343 intron variant T/G snv 0.39 4
rs16890979
SLC2A9
0.827 0.200 4 9920543 missense variant C/T snv 0.24 0.29 4
rs4698036 0.925 0.120 4 10329670 intergenic variant T/G snv 0.21 4
rs6855911
SLC2A9
0.851 0.200 4 9934286 intron variant A/G snv 0.33 4
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 4
rs737267
SLC2A9
0.851 0.240 4 9933120 intron variant G/A;T snv 4
rs7442295
SLC2A9
0.925 0.120 4 9964756 intron variant A/G snv 0.28 4
rs7671266
SLC2A9
0.925 0.120 4 10054752 intron variant T/C snv 0.73 4
rs9291683 0.925 0.120 4 10322536 intergenic variant G/A;C;T snv 4