Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113851554
MEIS1
0.882 0.080 2 66523432 intron variant G/A;T snv 5
rs12140153
PATJ
1 62114219 missense variant G/A;T snv 4.0E-06; 5.9E-02 5
rs11684176
PLCL1
2 198090050 intron variant C/T snv 0.38 3
rs1595824
PLCL1
2 198009282 intron variant C/A;T snv 3
rs3122163
HCRTR2
6 55191570 intron variant C/T snv 0.85 2
rs62158211
LOC101927400
2 113348562 intron variant G/T snv 0.18 2
rs76681500
LOC105378808
1 77247749 upstream gene variant G/A snv 0.11 2
rs694383
RGS16
1 182599069 3 prime UTR variant G/C snv 0.96 2
rs10194961 2 105687806 intergenic variant T/A;C snv 1
rs10493596 1 77260556 intergenic variant C/T snv 0.23 1
rs10896109 11 66312552 upstream gene variant A/G snv 0.58 1
rs11139851 9 82878125 intergenic variant C/G snv 0.28 1
rs12310956 12 33817747 intergenic variant A/G;T snv 1
rs12547604 8 5002969 intergenic variant G/C snv 0.18 1
rs12822662 12 38469868 regulatory region variant G/C snv 0.20 1
rs142398474 11 18647581 intergenic variant C/G;T snv 1
rs148750727 4 187101798 intergenic variant T/G snv 3.4E-03 1
rs17311976 8 130625091 intron variant T/C snv 0.13 1
rs190135744 4 32917220 intergenic variant C/T snv 1
rs192534763 8 36345428 intergenic variant T/C snv 6.1E-03 1
rs1969363 12 38121070 intergenic variant G/A;C snv 1
rs2050122 1 19662712 upstream gene variant T/C;G snv 1
rs2197308 12 37887459 intergenic variant A/G snv 0.39 1
rs2948276 7 96827807 TF binding site variant A/G;T snv 0.29 1
rs4295623 8 11665275 intergenic variant C/T snv 0.63 1