Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12369214
RIC8B
0.807 0.120 12 106804833 intron variant G/A snv 0.41 1
rs6720394
MIR4435-2HG
0.925 0.040 2 111231795 intron variant T/G snv 0.11 1
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs7937682
PPP2R1B ; SIK2
0.925 0.040 11 111709215 intron variant G/A;C snv 1
rs415595
LOC105371082 ; RMI2 ; TNP2
1.000 0.040 16 11269835 intron variant A/G snv 0.46 1
rs633683
PHLDB1
1.000 0.040 11 118634025 non coding transcript exon variant T/C snv 0.58 1
rs13132245 1.000 0.040 4 122128437 intergenic variant A/G snv 0.11 1
rs13151961
KIAA1109
0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs13119723
KIAA1109
0.807 0.280 4 122297158 intron variant A/G snv 0.10 5
rs13140464 0.925 0.040 4 122578590 regulatory region variant G/T snv 0.10 1
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 5
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 3
rs4391646
LOC112268276
1.000 0.040 1 166208147 intron variant T/C snv 0.22 1
rs6678400
LOC112268276
1.000 0.040 1 166208523 intron variant G/T snv 0.22 1
rs7426056 0.807 0.120 2 203747335 regulatory region variant A/G snv 0.81 1
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
rs3749171
GPR35
0.807 0.120 2 240630275 missense variant C/T snv 0.16; 9.4E-06 0.19 1
rs3748816
MMEL1
0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs2844559 1.000 0.040 6 31372298 intron variant C/T snv 8.0E-02 1
rs3099844
MICB-DT
0.732 0.400 6 31481199 non coding transcript exon variant C/A snv 0.11 9
rs2836883 0.882 0.080 21 39094818 intergenic variant G/A snv 0.23 1
rs11203203
UBASH3A
0.807 0.240 21 42416077 intron variant G/A snv 0.28 5
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 5
rs60652743
PRKD2
0.925 0.040 19 46702450 intron variant A/G snv 0.16 1