Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3810291 19 47065746 3 prime UTR variant G/A snv 0.50 9
rs10408163 19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs2303108 19 47086638 intron variant T/C snv 0.63 3
rs12973221 19 47111403 intron variant C/A snv 7.6E-02 2
rs2241388 19 47069730 intron variant T/C snv 0.62 2
rs113125564 19 47092874 intron variant T/C snv 2.9E-02 1
rs17716478 19 47097336 intron variant C/T snv 5.3E-02 1
rs62135070 19 47112578 missense variant C/T snv 3.7E-02 3.1E-02 1