Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4666002
ZNF512
0.925 0.120 2 27617773 intron variant G/A;C snv 6
rs2851682
FADS2
11 61848540 intron variant A/G snv 9.9E-02 5
rs174455
FADS3
1.000 0.080 11 61888645 intron variant G/A;C snv 5
rs174528
TMEM258 ; MYRF
1.000 0.080 11 61776027 intron variant T/C snv 0.42 0.42 5
rs3756963
ELOVL2
0.882 0.200 6 11021921 intron variant T/C snv 0.24 4
rs2072114
FADS2
1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16 4
rs334809
IL5RA
0.925 0.080 3 3088537 intron variant A/G;T snv 4
rs11667159 19 46291989 intergenic variant C/A;T snv 3
rs11668290 19 46292921 upstream gene variant G/A snv 0.12 3
rs11671319 19 46291810 intergenic variant T/C snv 0.12 3
rs11671360 19 46291914 intergenic variant T/C snv 0.12 3
rs11671710 19 46288677 regulatory region variant C/G;T snv 3
rs117366905 19 46294033 upstream gene variant A/G snv 0.12 3
rs117992292 19 46294038 upstream gene variant A/G snv 0.12 3
rs141332218 19 46293976 upstream gene variant T/C snv 0.12 3
rs142815467 19 46291277 intergenic variant -/T delins 0.12 3
rs174448 1.000 0.120 11 61872101 downstream gene variant G/A snv 0.61 3
rs34128150 19 46291852 intergenic variant C/A snv 0.12 3
rs7254961 19 46292627 upstream gene variant C/T snv 0.12 3
rs7256047 19 46292776 upstream gene variant T/C snv 0.12 3
rs73059722 19 46293161 upstream gene variant G/A snv 0.12 3
rs73059723 19 46293245 upstream gene variant A/C snv 0.12 3
rs73059724 19 46293510 upstream gene variant T/C snv 0.11 3
rs73059725 19 46293511 upstream gene variant G/A snv 0.11 3
rs73059726 19 46293937 upstream gene variant G/A snv 0.12 3