Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80095739 19 46282441 regulatory region variant A/G snv 0.10 3
rs9393800 6 10951504 intron variant A/G snv 0.20 3
rs10885997 10 116638460 synonymous variant A/G snv 0.38 0.36 2
rs11190604 10 100542700 intron variant A/G snv 0.19 2
rs12098564 10 85193571 non coding transcript exon variant A/G snv 7.4E-02 2
rs138572223 18 50446052 intergenic variant A/G snv 5.7E-03 2
rs174464 11 61890454 intron variant A/G snv 0.59 2
rs174472 11 61904484 intron variant A/G snv 0.41 2
rs17648246 13 44919746 intergenic variant A/G snv 5.0E-02 2
rs2727266 11 61936862 upstream gene variant A/G snv 9.8E-02 2
rs3798722 6 11040190 intron variant A/G snv 0.39 2
rs535211063 18 50009408 intron variant A/G snv 1.0E-03 2
rs1145652 5 165337081 intergenic variant A/G snv 9.6E-02 1
rs1225736 6 10939156 intron variant A/G snv 0.24 1
rs1570069 6 11017592 intron variant A/G snv 0.54 1
rs16832011
LCT
2 135787729 downstream gene variant A/G snv 5.1E-02 1
rs197770 3 37474336 intron variant A/G snv 0.12 1
rs2147041 6 11050290 intron variant A/G snv 0.53 1
rs2281591 6 10990260 intron variant A/G snv 0.30 1
rs2295600 6 10962017 intron variant A/G snv 0.45 1
rs2453710 11 61639070 non coding transcript exon variant A/G snv 0.45 1
rs2585617 6 68627895 non coding transcript exon variant A/G snv 0.90 1
rs3798709 6 11001043 intron variant A/G snv 0.18 1
rs6456745 6 10894035 intron variant A/G snv 0.36 0.38 1
rs695867 11 61793816 intron variant A/G snv 2.6E-02 1