Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs886424 0.744 0.250 6 30814225 non coding transcript exon variant C/T snp 7.1E-02 9.1E-02 16
rs1006737 0.679 0.107 12 2236129 intron variant G/A snp 0.37 13
rs8321 0.734 0.250 6 30064745 3 prime UTR variant A/C snp 5.4E-02 6.5E-02 13
rs2524005 0.821 0.036 6 29931900 intron variant G/A snp 0.17 11
rs4650608 0.801 0.036 1 78772330 intergenic variant T/C snp 0.31 11
rs10275045 0.801 0.143 7 1881190 intron variant C/T snp 0.33 11
rs1480380 0.744 0.321 6 32945469 intron variant C/T snp 0.11 10
rs17693963 0.821 0.036 6 27742386 intergenic variant A/C,G snp 6.4E-02 10
rs17746001 0.821 0.036 4 179734472 intergenic variant C/T snp 4.4E-02 10
rs9834970 0.821 0.036 3 36814539 intergenic variant T/C snp 0.44 10
rs6484218 0.801 0.036 11 10369034 intron variant G/A snp 0.21 10
rs4356203 0.821 0.036 11 17138601 intron variant A/G snp 0.33 10
rs7872515 0.821 0.036 9 92060258 intron variant G/A snp 0.24 10
rs7219021 0.821 0.036 17 48763179 intron variant T/G snp 0.24 10
rs12201676 0.821 0.036 6 89022382 intergenic variant T/C snp 0.21 8
rs802568 0.821 0.036 7 146262151 intron variant T/G snp 0.16 8
rs11789399 0.801 0.036 9 118597008 intergenic variant G/A,C snp 0.35 8
rs11191580 0.821 0.036 10 103146454 intron variant T/C snp 8.2E-02 8
rs9275524 0.784 0.143 6 32707332 intergenic variant T/C snp 0.57 7
rs174576 1.000 0.036 11 61836038 intron variant C/A,T snp 0.36 6
rs2252865 0.821 0.036 1 8362616 intron variant T/C snp 0.71 6
rs506597 0.878 0.036 7 100715797 intergenic variant A/G snp 0.89 5
rs7004633 0.821 0.036 8 88748082 intergenic variant A/G snp 0.26 5
rs9951150 0.821 0.036 18 55153893 intergenic variant A/G,T snp 0.50 5
rs10994359 0.801 0.036 10 60462349 intron variant T/C snp 9.2E-02 5