Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2742976
E2F2
0.882 0.240 1 23531510 upstream gene variant T/A;G snv 3
rs2281997
ENHO
0.882 0.240 9 34521869 intron variant T/A;C snv 5
rs150393409
FAN1
0.882 0.200 15 30910758 missense variant G/A;C snv 6.6E-03; 6.0E-05 3
rs3512
FAN1 ; MTMR10
0.925 0.160 15 30942802 3 prime UTR variant G/C snv 0.27 4
rs4746
GLO1
0.708 0.400 6 38682852 missense variant T/A;G snv 0.36 21
rs1806201
GRIN2B
0.776 0.200 12 13564574 synonymous variant G/A snv 0.32 0.24 8
rs1419046
GRK4
1.000 0.120 4 2984322 intron variant T/A snv 0.39 1
rs2471336
GRK4
1.000 0.120 4 2995884 intron variant T/C snv 0.32 1
rs2857845
GRK4
1.000 0.120 4 3026386 intron variant A/T snv 0.11 1
rs2960308
GRK4
1.000 0.120 4 2989313 intron variant G/A snv 0.48 1
rs2297235
GSTO2
0.752 0.320 10 104274733 5 prime UTR variant A/G snv 0.22 11
rs4523977
HAP1
1.000 0.120 17 41727098 missense variant G/A snv 0.23 0.18 1
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
rs110501
HTT
1.000 0.120 4 3223751 intron variant T/C snv 0.47 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
rs2071655
HTT
1.000 0.120 4 3116389 intron variant T/A;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
rs2471347
HTT
1.000 0.120 4 3042708 intron variant G/A snv 0.68 1
rs363066
HTT
1.000 0.120 4 3134226 intron variant T/A;G snv 1