Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10038113 1.000 0.040 5 25902233 intergenic variant T/C snv 0.45 1
rs10058083 1.000 0.040 5 25894289 intergenic variant G/A snv 0.38 1
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs10185592
LOC105373847
1.000 0.040 2 205829457 intergenic variant A/C snv 0.11 1
rs10205350
GALNT14
1.000 0.040 2 30923631 intron variant G/T snv 0.24 1
rs10239799 1.000 0.040 7 120765281 intergenic variant C/T snv 0.37 1
rs10489525
CSDE1
1.000 0.040 1 114721064 intron variant G/A snv 0.32 1
rs10498676
ELOVL2
0.925 0.040 6 11026766 intron variant G/A snv 0.18 1
rs10513025 1.000 0.040 5 9623510 non coding transcript exon variant T/C snv 5.4E-02 1
rs1057518345
ADNP
0.742 0.400 20 50894172 frameshift variant ACTA/- delins 25
rs1057518658
SCN2A
1.000 0.040 2 165331409 frameshift variant AC/- del 1
rs1057518993
IQSEC2
1.000 0.040 X 53243367 stop gained G/A snv 1
rs1057518999
FOXP1
1.000 0.040 3 70977826 splice donor variant A/G snv 1
rs1057519440
GSPT2
1.000 0.040 X 51744647 missense variant G/A snv 3
rs1057521223
SCN2A
1.000 0.040 2 165373339 stop gained G/A;T snv 5
rs1060499733
DHX30
0.851 0.120 3 47846757 missense variant A/G snv 11
rs1064793345
PTEN
0.752 0.240 10 87961039 missense variant T/C snv 10
rs1064794254
UPF3B
0.851 0.120 X 119841185 frameshift variant CT/- delins 6
rs10749886 1.000 0.040 11 107129809 intergenic variant G/A snv 0.35 1
rs1085307845
PHIP
0.752 0.320 6 79025582 missense variant G/T snv 21
rs1085307993
GABRB2
0.716 0.440 5 161331056 missense variant C/T snv 53
rs10858047 1.000 0.040 1 114531255 upstream gene variant T/C snv 0.13 1
rs10904487 1.000 0.040 10 5382502 intergenic variant C/T snv 0.64 1
rs10942147
MSNP1
1.000 0.040 5 25910820 non coding transcript exon variant G/A snv 0.27 1
rs11102800
TRIM33
1.000 0.040 1 114498310 intron variant C/T snv 0.58 2