Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555910162
SHANK3
0.925 0.080 22 50721469 frameshift variant -/C delins 5
rs951436 0.925 0.040 1 163063552 regulatory region variant A/C snv 0.42 3
rs2789588 6 72433995 intergenic variant A/C snv 0.26 1
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs9960767
TCF4
0.925 0.040 18 55487771 intron variant A/C;G snv 3
rs2509843 11 98254676 intergenic variant A/C;G;T snv 2
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1799990
PRNP
0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs737865
TXNRD2 ; COMT
0.763 0.240 22 19942598 intron variant A/G snv 0.23 11
rs187269
GABRB2
0.827 0.160 5 161329618 3 prime UTR variant A/G snv 0.34 6
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 6
rs2236418
GAD2
0.882 0.120 10 26216567 upstream gene variant A/G snv 0.36 6
rs61749465
MCPH1
0.851 0.120 8 6414832 missense variant A/G snv 2.1E-03 1.9E-03 5
rs6465084
LOC105375382 ; GRM3
0.851 0.040 7 86774159 intron variant A/G snv 0.26 5
rs12836771
HTR2C ; MIR1912 ; MIR1264
0.882 0.080 X 114650913 intron variant A/G snv 0.12 4
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
rs701428
RTN4R
1.000 0.040 22 20241019 downstream gene variant A/G snv 0.56 4
rs4309482
LOC105372125
0.925 0.040 18 55083238 intergenic variant A/G snv 0.39 3
rs7687423
NPY1R
0.925 0.080 4 163329645 intron variant A/G snv 0.53 3
rs7759855 0.925 0.040 6 28315086 downstream gene variant A/G snv 2.8E-02 3