Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs111412755 11 69973033 regulatory region variant C/T snv 0.12 1
rs111499603 3 47547159 intergenic variant C/G;T snv 1
rs11159096 14 74631610 regulatory region variant A/G snv 0.43 1
rs11187142 10 92708928 downstream gene variant T/C snv 0.80 1
rs11210029 1 41399621 regulatory region variant A/G;T snv 1
rs112184198 10 100844757 intergenic variant G/A snv 9.3E-02 1
rs11229252 11 55362164 intergenic variant C/T snv 8.7E-02 1
rs11240656 1 204069017 intron variant G/A snv 0.46 1
rs11252344 10 4101743 regulatory region variant C/T snv 5.9E-02 1
rs11263441 11 69437232 downstream gene variant G/A snv 0.11 1
rs112639668 6 31366162 upstream gene variant A/G snv 1
rs113044050 14 103541414 downstream gene variant C/T snv 0.13 1
rs113744258 12 65979721 intergenic variant T/G snv 0.51 1
rs11399965 3 134286877 intergenic variant AA/-;A;AAA;AAAA;AAAAA delins 1
rs114022259 4 54112440 intron variant C/G snv 6.2E-03 1
rs11525445 11 55583531 intergenic variant C/A;T snv 1
rs115381894 11 109148291 intergenic variant G/A snv 5.7E-03 1
rs11592107 10 121209450 intergenic variant G/A snv 0.23 1
rs11608075 11 107202560 intergenic variant A/G;T snv 1
rs11632436 15 85752055 intron variant G/A;C snv 0.39 1
rs11653623 17 8299302 upstream gene variant G/C snv 0.18 1
rs11679072 2 239522525 intron variant C/A snv 3.9E-02 1
rs116861740 21 16671610 intergenic variant G/C snv 1.1E-03 1
rs117212336 11 2095084 regulatory region variant C/T snv 3.0E-02 1
rs11721984 4 38342314 intergenic variant C/T snv 0.32 1