Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6457374 0.851 0.200 6 31304484 intron variant C/T snv 0.81 7
rs9368699 0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 7
rs2260000 0.851 0.200 6 31625699 intron variant A/G snv 0.29 6
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 6
rs6906846 0.851 0.280 6 31277959 non coding transcript exon variant A/G snv 0.67 6
rs12191877 0.851 0.120 6 31285148 intron variant C/T snv 0.12 5
rs4148325 0.851 0.080 2 233764663 intron variant C/T snv 0.36 3
rs2247056 0.882 0.160 6 31297713 intron variant T/C snv 0.80 8
rs2516509 0.882 0.160 6 31482217 intron variant T/C snv 0.19 7
rs2156875 0.882 0.200 6 31349570 intron variant C/T snv 0.50 6
rs2534657 0.882 0.200 6 31504682 intron variant C/T snv 0.15 6
rs259919 0.882 0.080 6 30057726 intron variant G/A snv 0.25 6
rs2736172 0.882 0.160 6 31623121 non coding transcript exon variant C/T snv 0.41 0.29 6
rs2844509 0.882 0.160 6 31543147 intron variant A/G snv 0.23 6
rs2856997 0.882 0.200 6 32813999 non coding transcript exon variant C/A snv 0.45 6
rs2894207 0.882 0.160 6 31295974 intron variant T/C snv 0.20 6
rs3130473 0.882 0.160 6 31231431 intergenic variant C/T snv 0.23 6
rs6906662 0.882 0.200 6 32298729 intron variant G/A snv 6.8E-02 6
rs241448 0.882 0.200 6 32828908 stop lost A/G snv 0.32 0.27 5
rs241453 0.882 0.160 6 32828449 3 prime UTR variant G/A snv 0.25 5
rs2517459 0.882 0.160 6 30929245 downstream gene variant T/C snv 0.74 5
rs8192591 0.882 0.160 6 32218019 missense variant C/T snv 2.5E-02 2.2E-02 5
rs9469003 0.882 0.160 6 31440051 intron variant T/C snv 0.22 5
rs8283 0.882 0.120 6 32115523 3 prime UTR variant A/G snv 0.25 4
rs9391734 0.882 0.160 6 32130206 5 prime UTR variant G/A snv 0.11 4