Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs78087832 0.925 0.040 2 224600060 intergenic variant C/T snv 2.4E-03 3
rs77945277 0.925 0.040 14 34840969 intron variant A/G snv 4.9E-03 3
rs77607745 1.000 0.040 13 69001052 intergenic variant A/C snv 0.15 2
rs7714426 1.000 0.040 5 120683373 intron variant C/A;G;T snv 2
rs7713917 0.925 0.040 5 79533426 upstream gene variant A/G snv 0.54 1
rs77087420 1.000 0.040 4 122201701 intron variant A/G snv 3.4E-02 2
rs76923064 1.000 0.040 2 156300636 downstream gene variant T/C snv 1.2E-02 2
rs7613360 1.000 0.040 3 49879277 upstream gene variant C/T snv 0.32 3
rs75995702 0.925 0.040 11 42785177 intergenic variant C/G;T snv 3
rs7597593 0.827 0.160 2 184668853 intron variant T/C snv 0.53 2
rs7583068 1.000 0.040 2 211769383 intron variant T/A snv 0.33 2
rs75650221 1.000 0.040 1 174452856 intron variant C/T snv 4.1E-02 2
rs75507262 1.000 0.040 1 229213737 intergenic variant A/G snv 8.0E-03 2
rs754593 1.000 0.040 17 45977330 non coding transcript exon variant G/A snv 0.52 4
rs7502590 1.000 0.040 17 81108281 non coding transcript exon variant A/G snv 0.14 2
rs74860738 0.925 0.040 11 80671683 intergenic variant G/A snv 7.2E-02 3
rs74338595 1.000 0.040 2 211885061 intron variant T/C snv 0.23 2
rs73788091 1.000 0.040 5 133429517 intron variant C/T snv 0.10 3
rs73720034 1.000 0.040 7 125794995 intergenic variant T/C snv 7.2E-02 3
rs73425402 0.925 0.040 12 77503518 intron variant T/A snv 4.1E-02 3
rs72995548 1.000 0.040 11 113268199 non coding transcript exon variant C/T snv 3.5E-02 2
rs72789910 1.000 0.040 2 24165740 intron variant T/G snv 0.17 2
rs72788286 1.000 0.040 2 23875451 intron variant A/C snv 0.12 2
rs7225384 1.000 0.040 17 45731730 non coding transcript exon variant C/G snv 0.39 2
rs7225002 0.925 0.080 17 46111701 intron variant A/G snv 0.39 7