Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1452075
CADPS
1.000 0.040 3 62495388 intron variant C/T snv 0.73 4
rs526126
FADS2
1.000 0.040 11 61857413 intron variant G/C;T snv 0.81; 8.0E-06 3
rs750257282
CARS1 ; CARS1-AS1
1.000 0.040 11 3038127 missense variant C/G;T snv 3.2E-05 3
rs10230087
FOXP2
1.000 0.040 7 114614352 intron variant G/A snv 0.73 2
rs10497655
LOC105373780 ; ZNF804A
1.000 0.040 2 184597314 intron variant T/C;G snv 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
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
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
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
rs199473391
CACNA1C
1.000 0.040 12 2607117 stop gained G/A;T snv 2
rs2061183
FOXP2
1.000 0.040 7 114617959 intron variant C/G snv 0.73 2
rs2289195
DNMT3A
1.000 0.040 2 25240614 intron variant G/A snv 0.41 0.41 2
rs251684
PLA2G4C
1.000 0.040 19 48098197 synonymous variant T/C snv 0.61 0.64 2
rs2898883
PHB
1.000 0.040 17 49405591 intron variant G/A snv 0.23 2
rs4541
CYP11B1 ; GML
1.000 0.040 8 142875277 missense variant G/A;T snv 7.8E-02; 2.0E-05 2
rs7632287
CAV3
1.000 0.040 3 8749760 intron variant G/A snv 0.32 2
rs9468304
ELOVL2-AS1 ; ELOVL2
1.000 0.040 6 11041932 intron variant G/A snv 0.19 2