Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114633080 1.000 0.080 6 145083119 intergenic variant G/A snv 4.2E-02 1
rs115045402 1.000 0.080 1 152057072 intergenic variant G/A snv 1.7E-02 1
rs115664621 1.000 0.080 6 32490013 intergenic variant A/G snv 0.30 1
rs115958457 1.000 0.080 16 86793401 intergenic variant C/T snv 9.2E-03 1
rs11602802 1.000 0.080 11 1139459 regulatory region variant C/A snv 0.54 1
rs116189786 1.000 0.080 6 32625900 upstream gene variant A/G snv 1.2E-03 1
rs116201499 1.000 0.080 16 13813303 intergenic variant G/A snv 8.8E-03 1
rs116278466 1.000 0.080 6 75236034 downstream gene variant G/A;T snv 1
rs11658582 1.000 0.080 17 40606948 TF binding site variant C/A;G;T snv 1
rs11666341 1.000 0.080 19 52098146 upstream gene variant G/A snv 0.18 1
rs11877305 1.000 0.080 18 77739121 intergenic variant G/A snv 7.0E-02 1
rs12143327 1.000 0.080 1 112068273 intergenic variant G/A snv 6.7E-02 1
rs1229598 1.000 0.080 18 56267556 regulatory region variant A/C;G;T snv 1
rs12568266 1.000 0.080 1 4133491 intergenic variant G/A;T snv 0.12 1
rs12718488 1.000 0.080 11 76655646 intron variant T/G snv 0.33 1
rs12785018 1.000 0.080 10 8473385 downstream gene variant C/T snv 0.36 1
rs13022699 1.000 0.080 2 101671373 intergenic variant C/T snv 5.3E-02 1
rs13263709 1.000 0.080 8 80374940 intron variant T/C snv 0.60 1
rs13405366 1.000 0.080 2 13542679 intron variant G/A snv 8.5E-02 1
rs1353649 1.000 0.080 11 20232053 intergenic variant A/G snv 0.69 1
rs139088362 1.000 0.080 6 32571334 intergenic variant T/A snv 1
rs139939994 1.000 0.080 9 6380605 intergenic variant C/G snv 5.0E-03 1
rs1412426 1.000 0.080 9 6188652 intergenic variant A/C;T snv 1
rs141602583 1.000 0.080 8 6333897 intergenic variant G/C snv 8.9E-03 1
rs1440095 1.000 0.080 2 42062526 downstream gene variant T/C snv 0.45 1