Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10497655
LOC105373780 ; ZNF804A
1.000 0.040 2 184597314 intron variant T/C;G snv 2
rs10951154
HOTAIRM1 ; HOXA1
0.925 0.040 7 27095695 missense variant C/A;G;T snv 0.76 2
rs1163276899
CACNA1D
1.000 0.040 3 53673125 missense variant G/A snv 2
rs11787216 1.000 0.040 8 141605122 intron variant C/T snv 0.26 2
rs12037377
TFB2M
1.000 0.040 1 246551218 missense variant G/A snv 3.2E-03 1.6E-03 2
rs121908445
CNTNAP2
0.925 0.040 7 148147542 missense variant T/C snv 3.3E-04 1.7E-04 2
rs12531289
FOXP2
1.000 0.040 7 114600061 intron variant T/A snv 0.73 2
rs12603582
ITGB3
1.000 0.040 17 47300211 intron variant G/T snv 0.18 2
rs1275980031
RELN
1.000 0.040 7 103540259 missense variant G/A snv 4.0E-06 2
rs13000344 0.925 0.040 2 63062599 downstream gene variant T/G snv 0.11 2
rs13294439 1.000 0.040 9 23358877 intron variant A/C snv 0.32 2
rs1350135
FOXP2
1.000 0.040 7 114602621 intron variant C/A;G;T snv 2
rs1477437491
NOS1AP
0.925 0.040 1 162367213 missense variant G/A snv 2.8E-05 2
rs1553518509
MBD5
1.000 0.040 2 148468916 stop gained C/T snv 2
rs17606561
ELOVL2
1.000 0.040 6 10982126 3 prime UTR variant G/A snv 0.17 2
rs1801291
MAOA
1.000 0.040 X 43744144 synonymous variant T/C snv 2
rs1804197
APC
1.000 0.040 5 112844212 3 prime UTR variant C/A snv 7.2E-02 2
rs1861972
EN2
0.925 0.040 7 155461298 intron variant G/A snv 0.72 2
rs1861973
EN2
0.925 0.040 7 155461450 intron variant T/C snv 0.73 2
rs1881084
SND1
0.925 0.040 7 127704626 intron variant G/A snv 0.33 2
rs1912960
GABRA4
0.925 0.040 4 46951864 intron variant G/C snv 0.28 2
rs199473391
CACNA1C
1.000 0.040 12 2607117 stop gained G/A;T snv 2
rs2018650
LOC100132215 ; EHBP1
0.925 0.040 2 63045589 3 prime UTR variant T/C snv 0.11 2
rs2061183
FOXP2
1.000 0.040 7 114617959 intron variant C/G snv 0.73 2
rs2278556
ATP2B2
0.925 0.040 3 10360419 intron variant G/A snv 0.34 2