Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121917767
UCHL1
0.827 0.120 4 41260751 missense variant C/A;G;T snv 4.0E-05; 4.0E-06; 2.0E-05 6
rs10937921 1.000 0.120 4 3274764 downstream gene variant C/T snv 0.40 2
rs1277892620
ACACA
0.925 0.120 17 37242036 synonymous variant A/G snv 4.0E-06 7.0E-06 2
rs2798224
MSANTD1
1.000 0.120 4 3265941 intron variant G/A snv 0.45 2
rs362272
HTT
1.000 0.120 4 3233253 missense variant G/A;T snv 0.29 2
rs363092
HTT
1.000 0.120 4 3194302 intron variant A/C;T snv 0.51 2
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
rs10934657
KALRN
1.000 0.120 3 124093989 intron variant T/C snv 0.60 1
rs110501
HTT
1.000 0.120 4 3223751 intron variant T/C snv 0.47 1
rs11248108
RNF4
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
rs1170668763
BECN1
1.000 0.120 17 42818395 missense variant T/A snv 7.0E-06 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
rs1232027
LINC01337
1.000 0.120 5 80619201 intron variant G/A snv 0.32 1
rs12641989
RGS12
1.000 0.120 4 3418113 non coding transcript exon variant G/A;C snv 1
rs12668183 1.000 0.120 7 16455781 regulatory region variant T/C snv 0.34 1
rs13102260
HTT-AS ; HTT
1.000 0.120 4 3074678 intron variant G/A snv 0.15 1
rs1313770
HTT-AS ; HTT
1.000 0.120 4 3056082 intron variant A/G snv 0.57 1
rs1419046
GRK4
1.000 0.120 4 2984322 intron variant T/A snv 0.39 1
rs16844309
RGS12
1.000 0.120 4 3416539 intron variant G/A snv 0.26 1
rs1730768
RGS12
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
LOC107986321 ; NPY2R
1.000 0.120 4 155208405 non coding transcript exon variant A/C;G snv 1