Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000592 1.000 0.040 2 118939624 upstream gene variant C/A snv 6.4E-03 1
rs1000952
HTR3D
1.000 0.040 3 184038034 missense variant G/A;C;T snv 0.66; 3.6E-05; 4.0E-06 1
rs10042486 0.882 0.040 5 63965502 intron variant C/T snv 0.58 4
rs10070190 0.925 0.040 5 26866262 intergenic variant G/A snv 0.60 2
rs10491734 1.000 0.040 9 4482706 intergenic variant T/A;C snv 1
rs1059004
OLIG2
0.925 0.040 21 33028155 3 prime UTR variant C/A snv 0.41 4
rs11149058
LOC105370269
0.925 0.120 13 76978136 downstream gene variant T/A;C;G snv 2
rs11174202
TAFA2
0.925 0.040 12 61858476 intron variant A/G snv 0.49 2
rs1148374
CDH2
1.000 0.040 18 28070318 intron variant T/A snv 0.31 1
rs11583978
DLGAP3
0.925 0.040 1 34864921 downstream gene variant A/C;G snv 2
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs11783752 0.925 0.040 8 20192013 intergenic variant G/A;C snv 2
rs11854486
TRPM7
1.000 0.040 15 50660473 intron variant T/C snv 7.3E-02 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12504244 0.925 0.040 4 54619021 intergenic variant C/A;G;T snv 2
rs12536521 1.000 0.040 7 89349373 intergenic variant T/A snv 4.8E-02 1
rs12605662
CDH2
1.000 0.040 18 28171702 intron variant G/A snv 0.48 1
rs12635725 1.000 0.040 3 1895465 intergenic variant A/G;T snv 1
rs1265692223
HTR3E ; LOC105374249 ; HTR3E-AS1
1.000 0.040 3 184100530 missense variant A/G snv 4.0E-06 1
rs12682807
SLC1A1 ; SPATA6L
1.000 0.040 9 4574022 splice region variant A/C snv 0.11 8.5E-02 1
rs13046814
LOC107985505 ; OLIG2
1.000 0.040 21 33029069 3 prime UTR variant T/G snv 0.26 1
rs13316193
CAV3 ; OXTR
0.882 0.040 3 8761057 intron variant T/C snv 0.45 4
rs1417182
GRIK2
1.000 0.040 6 101885466 intron variant G/A snv 0.40 1
rs1477437491
NOS1AP
0.925 0.040 1 162367213 missense variant G/A snv 2.8E-05 2
rs150504822
SLITRK1
1.000 0.040 13 83880256 missense variant T/A snv 1.3E-03 1.2E-03 1