Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 5
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 4
rs10905718 1.000 0.040 10 6072893 upstream gene variant A/G snv 0.25 1
rs13132245 1.000 0.040 4 122128437 intergenic variant A/G snv 0.11 1
rs1452787
TCF4
0.827 0.160 18 55539976 intron variant A/G snv 0.24 1
rs415595
LOC105371082 ; RMI2 ; TNP2
1.000 0.040 16 11269835 intron variant A/G snv 0.46 1
rs60652743
PRKD2
0.925 0.040 19 46702450 intron variant A/G snv 0.16 1
rs7426056 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 1
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs10883371
LINC01475 ; NKX2-3
1.000 0.040 10 99532698 upstream gene variant C/A snv 0.54 1
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 2
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 1
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 3
rs1788097
CD226
0.925 0.040 18 69876452 intron variant C/T snv 0.56 1
rs2844559 1.000 0.040 6 31372298 intron variant C/T snv 8.0E-02 1
rs3749171
GPR35
0.807 0.120 2 240630275 missense variant C/T snv 0.16; 9.4E-06 0.19 1
rs6971637
LOC101927243
1.000 0.040 7 77425403 non coding transcript exon variant C/T snv 7.1E-03 1
rs7791854 1.000 0.040 7 77427905 downstream gene variant C/T snv 3.3E-03 1
rs3197999
MST1 ; APEH
0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 5
rs12369214
RIC8B
0.807 0.120 12 106804833 intron variant G/A snv 0.41 1
rs17683107
GAS7
1.000 0.040 17 9921085 intron variant G/A snv 0.13 1