Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1428323 1.000 0.040 5 29911927 intergenic variant A/G snv 0.97 1
rs1593906 1.000 0.040 5 29914385 intergenic variant C/T snv 0.97 1
rs2335367
ZNF93
1.000 0.040 19 19913057 intron variant T/C snv 0.96 1
rs6855482
LOC100507053 ; ADH4
1.000 0.040 4 99135808 intron variant C/T snv 0.96 1
rs1427615
THSD7B
1.000 0.040 2 136783263 intron variant C/T snv 0.96 1
rs351596 1.000 0.040 1 4317851 intergenic variant C/T snv 0.96 1
rs337635
LOC102723415
1.000 0.040 4 38601651 downstream gene variant A/C snv 0.96 1
rs8108751
LOC101927151
1.000 0.040 19 27831740 intron variant T/A snv 0.96 1
rs7207864
DPH1
1.000 0.040 17 2029022 upstream gene variant A/C snv 0.95 1
rs630340
LOC107985179
1.000 0.040 18 71505850 intergenic variant G/A snv 0.95 1
rs8027220 1.000 0.040 15 38199200 intron variant T/G snv 0.95 1
rs441869
ARHGEF33 ; LOC105374471
1.000 0.040 2 38951352 intron variant G/C snv 0.95 1
rs503100
POMGNT2 ; LOC107986079
1.000 0.040 3 43087416 intron variant A/T snv 0.95 1
rs262420
LDLRAD3
1.000 0.040 11 36014806 intron variant G/T snv 0.95 1
rs1812067 1.000 0.040 16 61023175 intergenic variant T/A snv 0.95 1
rs4822655
MYO18B
1.000 0.040 22 25790631 intron variant A/G snv 0.95 1
rs4316830
ARHGAP28
1.000 0.040 18 6762862 intron variant G/C snv 0.95 1
rs4832055 1.000 0.040 2 83697645 intergenic variant G/A snv 0.95 1
rs4883930 1.000 0.040 13 73299997 intergenic variant T/C snv 0.94 1
rs169715
LOC107986570
1.000 0.040 6 11938564 intergenic variant G/A snv 0.94 1
rs7451370 1.000 0.040 6 102632367 intergenic variant A/C snv 0.94 1
rs4907911 1.000 0.040 1 100562530 intergenic variant G/A snv 0.94 1
rs7093024 1.000 0.040 10 59769032 intergenic variant C/T snv 0.94 1
rs973236
DAB1
1.000 0.040 1 58304085 intron variant C/T snv 0.94 1
rs11642182
GP2
1.000 0.040 16 20311117 3 prime UTR variant A/G snv 0.94 1