Disease: Pseudocholinesterase Measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs660240
CELSR2
1 109275216 3 prime UTR variant T/C snv 0.75 5
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs10199768
APOB
2 21021128 intron variant G/T snv 0.35 5
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 7
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs10503669 0.925 0.080 8 19990179 intergenic variant C/A snv 8.4E-02 7
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs17410962 1.000 0.040 8 19990569 intergenic variant G/A snv 0.15 6
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 7
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 7
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs4775041
ALDH1A2
1.000 0.040 15 58382496 intron variant G/C snv 0.24 7
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20 5
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 5
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 7