Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12214131 0.807 0.080 6 105760046 intron variant G/A snv 0.29 7
rs1262557 0.807 0.080 6 126733443 intron variant C/T snv 0.51 7
rs12702271 0.807 0.080 7 46904161 intron variant C/T snv 0.20 7
rs13405699 0.807 0.080 2 173740905 intergenic variant C/A;G;T snv 7
rs201563 0.807 0.080 20 22019643 intergenic variant C/T snv 0.49 7
rs2180439 0.807 0.080 20 21872462 intergenic variant C/T snv 0.58 7
rs246180 0.807 0.080 16 14298066 upstream gene variant C/A;T snv 7
rs2497938 0.807 0.080 X 67343176 intergenic variant T/C snv 0.37 7
rs4718886 0.807 0.080 7 69433703 upstream gene variant A/G snv 0.27 7
rs58788673 0.807 0.080 7 46864701 intergenic variant -/CA ins 0.22 7
rs62060349 0.807 0.080 17 57153807 intergenic variant T/C snv 0.37 7
rs6625163 0.807 0.080 X 67291142 intergenic variant G/A snv 0.62 7
rs6752754 0.807 0.080 2 6429434 intergenic variant A/G snv 0.15 7
rs7534070 0.807 0.080 1 25171684 intergenic variant G/A;T snv 7
rs76972608 0.807 0.080 12 130078818 intergenic variant A/T snv 0.13 7
rs78003935 0.807 0.080 1 170372381 upstream gene variant T/A;G snv 0.25 7
rs79437808 0.807 0.080 8 108585572 intron variant C/T snv 1.3E-02 7
rs9287638 0.807 0.080 2 238785990 downstream gene variant C/A snv 0.40 7
rs9357047 0.807 0.080 6 9327323 intergenic variant T/A;C snv 7
rs12565727
C1orf127
0.807 0.080 1 10973025 intron variant A/G snv 0.31 7
rs2095921
C1orf127
0.807 0.080 1 10973265 intron variant C/G;T snv 7
rs7542354
C1orf127
0.807 0.080 1 10980328 intron variant G/A snv 0.37 7
rs13021718
DPY30 ; MEMO1
0.807 0.080 2 31956355 intron variant G/A snv 0.15 7
rs12902958
DRAIC
0.807 0.080 15 69747915 intron variant G/A snv 7.7E-02 7
rs7177657
DRAIC
0.807 0.080 15 69749354 intron variant T/C snv 8.7E-02 7