Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113851554
MEIS1
0.882 0.080 2 66523432 intron variant G/A;T snv 5
rs3810651
GABRQ ; LOC105373370
0.925 0.080 X 152652814 missense variant A/C;T snv 4
rs12469063
MEIS1
0.925 0.080 2 66537176 intron variant A/G snv 0.18 2
rs12593813
MAP2K5
1.000 0.080 15 67744514 intron variant A/G snv 0.53 2
rs3104767
CASC16
0.925 0.080 16 52590826 intron variant G/T snv 0.49 2
rs693534
NOS1
1.000 0.080 12 117346913 intron variant G/A snv 0.36 2
rs7977109
NOS1
1.000 0.080 12 117292535 intron variant G/A;T snv 2
rs10208712 1.000 0.080 2 3986856 regulatory region variant A/G snv 0.26 1
rs1026732
MAP2K5
1.000 0.080 15 67802747 intron variant G/A snv 0.38 1
rs10952927
LOC107986816
1.000 0.080 7 88729746 intron variant A/G;T snv 1
rs111652004 1.000 0.080 15 47068169 intergenic variant G/T snv 8.6E-02 1
rs11635424
MAP2K5
1.000 0.080 15 67745240 intron variant A/G snv 0.53 1
rs12046503 1.000 0.080 1 106652717 intergenic variant T/C snv 0.32 1
rs12450895
LINC02086
1.000 0.080 17 48695414 intron variant G/A snv 0.27 1
rs12962305
LINC01478
1.000 0.080 18 44290278 intron variant C/T snv 0.21 1
rs138915427
PTPRD
1.000 0.080 9 8341723 missense variant C/A;G;T snv 4.0E-06; 2.0E-05; 2.4E-05 1
rs17636328
LINC02520
1.000 0.080 6 37522755 intron variant A/G snv 0.14 1
rs1800652
FXN
1.000 0.080 9 69046200 intron variant G/A snv 0.24 1
rs1820989 1.000 0.080 2 67842758 intergenic variant A/C;G snv 1
rs1836229
PTPRD
1.000 0.080 9 8820573 intron variant A/C;G;T snv 1
rs1848460 1.000 0.080 3 3406460 intron variant A/T snv 0.33 1
rs1918752
UTRN
1.000 0.080 6 144587941 intron variant A/T snv 0.22 1
rs1975197
PTPRD
1.000 0.080 9 8846955 intron variant G/A snv 0.16 1
rs1983167 1.000 0.080 X 42989135 regulatory region variant T/C snv 1
rs2229940
GABRA4 ; GABRB1
1.000 0.080 4 46993349 missense variant G/T snv 0.32 0.31 1