Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4971100
TRIM46
0.925 0.120 1 155183255 intron variant G/A snv 0.39 2
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 1
rs12124078
DNAJC16
1 15543404 intron variant A/G snv 0.32 1
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 1
rs267738
CERS2
1.000 0.040 1 150968149 missense variant T/A;G snv 4.0E-06; 0.15 1
rs2842870
PMF1 ; PMF1-BGLAP
1 156230880 intron variant T/A;C snv 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 8
rs13538
NAT8 ; ALMS1P1
1.000 0.080 2 73641201 missense variant A/G snv 0.21 0.31 3
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 3
rs10206899
ALMS1P1
2 73673773 intron variant T/C;G snv 0.21; 3.9E-05 2
rs12989250
ORC4
0.925 0.120 2 148018869 intron variant G/A snv 0.32 2
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 2
rs4441471 1.000 0.080 2 16534140 intron variant A/G snv 0.41 1
rs6431731
LINC01804
1.000 0.080 2 15722878 intron variant C/T snv 0.97 1
rs807624 1.000 0.160 2 15642347 regulatory region variant G/T snv 0.47 1
rs16853722
MECOM
3 169432844 intron variant T/C snv 0.11 1
rs347685
TFDP2
1.000 0.080 3 142088295 intron variant C/A snv 0.74 1
rs6440003
ZBTB38
3 141375367 intron variant G/A snv 0.54 1
rs7624084
ZBTB38
3 141374443 intron variant T/C snv 0.54 1
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 3
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 3
rs17319721
SHROOM3
0.925 0.080 4 76447694 intron variant G/A snv 0.34 2