Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2268666
GRM1
1.000 0.040 6 146424952 intron variant C/T snv 0.51 1
rs772335034
P2RX2
1.000 0.040 12 132618851 missense variant C/A snv 9.6E-06 1
rs10233018 0.925 0.040 7 117883655 non coding transcript exon variant A/G snv 0.53 2
rs10485715 0.925 0.040 20 7279278 intergenic variant T/C snv 5.5E-02 2
rs10809520 0.925 0.040 9 11557797 intergenic variant C/T snv 0.28 2
rs195478 0.925 0.040 6 115851928 intergenic variant C/A;G snv 2
rs4685959 0.925 0.040 3 5645577 regulatory region variant C/G;T snv 2
rs4810896 0.925 0.040 20 48918761 upstream gene variant A/C;G snv 2
rs75921243 0.925 0.040 8 9988356 intron variant T/G snv 1.9E-02 2
rs76767803 0.925 0.040 3 36230378 intergenic variant C/T snv 0.16 2
rs116609693
ANKRD19P
0.925 0.040 9 92811394 intron variant C/T snv 6.1E-02 2
rs1961982
C12orf42
0.925 0.040 12 103218955 intergenic variant G/A snv 0.27 2
rs17156280
CACNA2D1
0.925 0.040 7 82414674 intron variant T/C snv 3.4E-02 2
rs7343
CMYA5
0.925 0.040 5 79799898 3 prime UTR variant G/A snv 0.13 2
rs1690818
CNTN5
0.925 0.040 11 99625823 intron variant C/T snv 0.61 2
rs62100776
DCC
0.925 0.040 18 53228263 intron variant A/T snv 0.35 2
rs319924
EYS ; PHF3
0.925 0.040 6 63777354 intron variant A/G;T snv 2
rs6320
HTR5A-AS1 ; HTR5A
0.925 0.040 7 155070911 synonymous variant T/A;G snv 0.26; 1.2E-05 2
rs2017122
KMT2A
0.925 0.040 11 118444134 intron variant C/T snv 4.0E-02 2
rs10884216
LINC02627
0.925 0.040 10 105701367 intergenic variant T/C snv 0.17 2
rs782212
LOC105378797
0.925 0.040 1 72479983 intron variant C/T snv 0.34 2
rs2551941
METTL21A
0.925 0.040 2 207627419 upstream gene variant A/G;T snv 2
rs3825882
NTRK3
0.925 0.040 15 88126151 intron variant G/C;T snv 2
rs4887379
NTRK3
0.925 0.040 15 88184105 intron variant C/G snv 0.24 2
rs2221540
OPCML
0.925 0.040 11 132846474 intron variant A/G snv 0.11 2