Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6855981
HTT
1.000 0.120 4 3146549 intron variant G/A snv 0.34 2
rs10015979
HTT
1.000 0.120 4 3107715 intron variant A/G snv 0.30 1
rs110501
HTT
1.000 0.120 4 3223751 intron variant T/C snv 0.47 1
rs11248108 1.000 0.120 4 2479763 intron variant G/A;T snv 1
rs1138690 1.000 0.120 4 3289674 upstream gene variant G/A;T snv 1
rs11731237
HTT
1.000 0.120 4 3150086 intron variant C/T snv 0.26 1
rs1210554604
HTT
1.000 0.120 4 3131662 missense variant G/A snv 1
rs12641989 1.000 0.120 4 3418113 non coding transcript exon variant G/A;C snv 1
rs13102260 1.000 0.120 4 3074678 intron variant G/A snv 0.15 1
rs1313770 1.000 0.120 4 3056082 intron variant A/G snv 0.57 1
rs1419046 1.000 0.120 4 2984322 intron variant T/A snv 0.39 1
rs16844309 1.000 0.120 4 3416539 intron variant G/A snv 0.26 1
rs1730768 1.000 0.120 4 3407632 intron variant A/G snv 0.85 1
rs2071655
HTT
1.000 0.120 4 3116389 intron variant T/A;G snv 1
rs2234759 1.000 0.120 4 155208405 non coding transcript exon variant A/C;G snv 1
rs2269499
HTT
1.000 0.120 4 3237975 intron variant C/T snv 0.24 1
rs2285086
HTT
1.000 0.120 4 3087532 intron variant A/G snv 0.48 1
rs2298969
HTT
1.000 0.120 4 3184517 intron variant A/G;T snv 1
rs2471336 1.000 0.120 4 2995884 intron variant T/C snv 0.32 1
rs2471347
HTT
1.000 0.120 4 3042708 intron variant G/A snv 0.68 1
rs2749782 1.000 0.120 4 3338034 intron variant T/C snv 0.70 1
rs2798296 1.000 0.120 4 3060438 intron variant A/G snv 0.44 1
rs2857845 1.000 0.120 4 3026386 intron variant A/T snv 0.11 1
rs2857861 1.000 0.120 4 3322040 intron variant C/T snv 0.53 1
rs2960308 1.000 0.120 4 2989313 intron variant G/A snv 0.48 1