Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs559802496 1.000 0.080 6 33098817 upstream gene variant A/G snv 1
rs6457713 1.000 0.080 6 33109999 upstream gene variant C/T snv 0.15 1
rs7741912 1.000 0.080 6 33058310 regulatory region variant C/G snv 0.29 1
rs7753264 1.000 0.080 6 32434663 intergenic variant A/G snv 0.38 1
rs7774047 1.000 0.080 6 32430786 intergenic variant C/A snv 0.38 1
rs86715 1.000 0.080 6 33512658 regulatory region variant A/G snv 0.27 1
rs9268589 1.000 0.080 6 32430425 intergenic variant G/A snv 0.38 1
rs9268608 1.000 0.080 6 32433088 intergenic variant C/T snv 0.38 1
rs9268613 1.000 0.080 6 32434915 upstream gene variant C/T snv 0.38 1
rs9271303 1.000 0.080 6 32613870 intergenic variant A/G snv 0.43 1
rs9271325 1.000 0.080 6 32614736 intergenic variant C/A;G snv 1
rs9275373 1.000 0.080 6 32700634 regulatory region variant G/A snv 0.12 1
rs9276302 1.000 0.080 6 32735429 upstream gene variant A/G;T snv 1
rs9380335 1.000 0.080 6 33057397 regulatory region variant C/G;T snv 1
rs9469325 1.000 0.080 6 33062664 downstream gene variant C/A snv 1
rs9469329 1.000 0.080 6 33063825 downstream gene variant C/T snv 0.31 1
rs11568695
ABCC4
1.000 0.080 13 95044286 synonymous variant C/T snv 1.2E-02 4.7E-02 1
rs9530614
ACOD1 ; LOC105370269
1.000 0.080 13 76953572 intron variant A/C;G snv 6.7E-06; 0.47 1
rs112120857
APOBEC3C ; APOBEC3F
1.000 0.080 22 39018377 missense variant G/C;T snv 5.2E-05; 5.4E-03 1
rs10485138
ASCC3
1.000 0.080 6 100690714 intron variant C/T snv 2.5E-02 1
rs2185379
ATG5 ; PRDM1
1.000 0.080 6 106088378 missense variant G/A snv 3.8E-02 4.5E-02 1
rs622502
CISH
1.000 0.080 3 50608362 intron variant C/A;G;T snv 5.1E-04; 0.89 1
rs369560944
DOCK11
1.000 0.080 X 118543579 synonymous variant T/C snv 5.5E-06 9.4E-06 1
rs760326374
EIF2AK2
1.000 0.080 2 37139666 missense variant C/A;T snv 4.0E-06; 4.0E-06 1
rs2836389
ERG
1.000 0.080 21 38431740 intron variant T/C snv 0.27 1