Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10747044 9 136424677 downstream gene variant G/T snv 0.26 1
rs10758392 9 36730777 intergenic variant T/G snv 0.56 1
rs10758394 9 36734255 intergenic variant A/G snv 0.58 1
rs10766035 11 13093570 intron variant C/A;G;T snv 1
rs10779201 12 85750094 intergenic variant A/G snv 0.67 1
rs10783130 1 100341341 upstream gene variant C/G snv 0.21 1
rs10784006 12 59862761 intergenic variant T/A snv 0.30 1
rs10786153 10 80955962 intergenic variant C/G snv 0.25 1
rs10792302 11 61128693 downstream gene variant T/A;C snv 1
rs10801266 1 193924556 intron variant G/A snv 0.37 1
rs10806538 6 66539184 intergenic variant A/G snv 0.54 1
rs10813357 9 30743642 intergenic variant G/A;T snv 1
rs10814435 9 36733159 intergenic variant C/T snv 0.56 1
rs10814436 9 36733239 intergenic variant A/G;T snv 1
rs10814437 9 36734003 intergenic variant C/A snv 0.58 1
rs10814438 9 36734491 intergenic variant G/A snv 0.58 1
rs10862034 12 80034325 downstream gene variant A/G snv 0.12 1
rs10863071 12 85752035 intergenic variant A/G snv 0.62 1
rs10888908 1 55260846 intron variant T/C;G snv 1
rs10894847 11 100385044 intergenic variant G/T snv 0.17 1
rs10897140 11 61128578 downstream gene variant C/A snv 0.57 1
rs10897181 11 61870762 downstream gene variant G/C snv 0.89 1
rs10897203 11 62011041 downstream gene variant A/C snv 0.99 1
rs10897209 11 62036068 regulatory region variant A/G;T snv 1
rs10912160 1 187742586 intergenic variant G/A snv 0.11 1