Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11098403 0.925 0.040 4 117725752 intergenic variant A/G snv 0.25 1
rs11102159 1.000 0.040 1 110782105 regulatory region variant C/T snv 0.31 1
rs11104379 1.000 0.040 12 87266212 regulatory region variant T/G snv 0.21 1
rs11127668 1.000 0.040 3 79866620 intergenic variant C/T snv 0.27 1
rs111364339 1.000 0.040 10 63098112 intergenic variant T/C snv 3.3E-02 1
rs111547017 1.000 0.040 6 43373951 intron variant A/G snv 7.5E-02 1
rs11165389 1.000 0.040 1 95350307 downstream gene variant T/G snv 0.33 1
rs111782145 1.000 0.040 6 30905731 upstream gene variant T/C snv 5.5E-02 1
rs1120004 1.000 0.040 12 23480498 intergenic variant T/G snv 0.60 1
rs112509803 1.000 0.040 7 24695385 downstream gene variant G/C;T snv 1
rs112973353 1.000 0.040 14 104071343 intergenic variant C/T snv 7.3E-02 1
rs114042773 1.000 0.040 5 125639572 intron variant T/A;C snv 1
rs114200269 1.000 0.040 6 30368886 upstream gene variant T/C snv 1
rs114377514 1.000 0.040 6 32793729 intergenic variant C/T snv 1
rs114540395 1.000 0.040 10 101719305 intron variant C/T snv 9.2E-02 1
rs11534004 1.000 0.040 7 113827389 intergenic variant A/G snv 0.18 1
rs11562926 1.000 0.040 4 117728887 intergenic variant T/C snv 0.29 1
rs11625793 1.000 0.040 14 65849165 intergenic variant G/A snv 0.46 1
rs116757206 1.000 0.040 6 29015497 intergenic variant G/C snv 1
rs11677416 1.000 0.040 2 112771663 downstream gene variant T/C snv 0.26 1
rs11680328 1.000 0.040 2 17856540 intergenic variant T/A snv 0.81 1
rs117019455 1.000 0.040 8 15796634 intergenic variant G/A snv 1.3E-02 1
rs11785400 1.000 0.040 8 142649072 intergenic variant T/A;C;G snv 1
rs11901793 1.000 0.040 2 236588594 intergenic variant A/G snv 0.38 1
rs1191551 1.000 0.040 14 29531199 intergenic variant T/G snv 0.82 1