Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4327572 0.882 0.120 5 25972712 intron variant C/T snv 0.28 3
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 2
rs4773054 1.000 0.040 13 109501681 intron variant T/C snv 0.89 2
rs6894838 0.925 0.080 5 25944837 intergenic variant T/C snv 0.63 2
rs10038113 1.000 0.040 5 25902233 intergenic variant T/C snv 0.45 1
rs10058083 1.000 0.040 5 25894289 intergenic variant G/A snv 0.38 1
rs10239799 1.000 0.040 7 120765281 intergenic variant C/T snv 0.37 1
rs10513025 1.000 0.040 5 9623510 non coding transcript exon variant T/C snv 5.4E-02 1
rs10749886 1.000 0.040 11 107129809 intergenic variant G/A snv 0.35 1
rs10858047 1.000 0.040 1 114531255 upstream gene variant T/C snv 0.13 1
rs10904487 1.000 0.040 10 5382502 intergenic variant C/T snv 0.64 1
rs11102807 1.000 0.040 1 114518963 intergenic variant A/G snv 0.44 1
rs11899372 1.000 0.040 2 127016304 upstream gene variant G/T snv 6.1E-02 1
rs12518194 1.000 0.040 5 25951452 intergenic variant A/G snv 0.27 1
rs12519594 1.000 0.040 5 25934696 intergenic variant G/A snv 0.27 1
rs12521157 1.000 0.040 5 25869292 intergenic variant C/T snv 0.28 1
rs12521388 1.000 0.040 5 25912004 downstream gene variant G/A snv 0.29 1
rs12701862 1.000 0.040 7 41083854 intergenic variant G/A snv 0.68 1
rs13166776 1.000 0.040 5 25971247 intron variant T/C snv 0.28 1
rs13176113 1.000 0.040 5 25900331 intergenic variant G/A snv 0.28 1
rs13187934 1.000 0.040 5 25902259 intergenic variant C/T snv 0.28 1
rs1346536 1.000 0.040 5 25915543 downstream gene variant A/G;T snv 1
rs1408744 1.000 0.040 6 23789887 intergenic variant A/G snv 0.63 1
rs17007739 1.000 0.040 4 83920097 intron variant T/G snv 0.38 1
rs17482975 1.000 0.040 5 25901499 intergenic variant C/T snv 0.28 1