Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10490120 2 48916690 intron variant A/G snv 9.3E-02 1
rs11218721 11 122634009 regulatory region variant C/A snv 0.37 1
rs114846969 19 11080521 downstream gene variant G/A snv 0.12 1
rs116376114 21 41884157 upstream gene variant T/C snv 8.2E-03 1
rs117492019 19 58170494 intron variant G/T snv 0.14 1
rs12151108 19 11086585 upstream gene variant G/A snv 0.12 1
rs13205804 6 32695620 intergenic variant A/G snv 0.13 1
rs13288021 9 19217423 intergenic variant C/T snv 6.6E-02 1
rs138108930 8 11938077 intron variant AATA/-;AATAAATA delins 1
rs139562989 17 8276406 upstream gene variant CAA/- delins 0.48 1
rs145859971 11 116817950 upstream gene variant G/A snv 1.9E-02 1
rs181946711 4 72608525 intergenic variant T/A snv 1.5E-03 1
rs181948526 4 72902905 intergenic variant G/T snv 1.5E-03 1
rs182472492 2 202624734 upstream gene variant A/G snv 0.26 1
rs192975004 4 72654548 intergenic variant T/C snv 2.7E-03 1
rs199987224 5 75269375 intergenic variant GTCTCCCTCTCCGTCTCCCTCTCC/-;GTCTCCCTCTCC delins 0.35 1
rs217386 7 44561096 downstream gene variant G/A snv 0.41 1
rs2218260 15 57922012 regulatory region variant T/C snv 0.36 1
rs2294261 6 16108932 downstream gene variant A/C snv 0.65 1
rs2587534 1 234713592 intron variant G/A snv 0.65 1
rs34318965 16 11537712 intergenic variant T/C snv 0.30 1
rs4002471 19 48711838 downstream gene variant C/T snv 0.39 1
rs4756996 11 19333933 intergenic variant C/T snv 0.21 1
rs484084 1 234721929 upstream gene variant T/C snv 0.66 1
rs537526354 4 72625905 intergenic variant G/A snv 1.5E-03 1