Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909224
PTEN
0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 29
rs121909219
PTEN
0.689 0.400 10 87957915 stop gained C/A;T snv 24
rs1085308043
PTEN
0.763 0.200 10 87925511 splice acceptor variant A/G;T snv 12
rs28934908
MECP2
0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 12
rs112795301
FOXP1
0.776 0.160 3 70972634 stop gained G/A snv 11
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs863225082
PPP2R5D ; MEA1
0.827 0.160 6 43007265 missense variant G/A snv 7
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs727504317
MAP2K1
0.807 0.320 15 66435145 missense variant G/A snv 6
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs1452075
CADPS
1.000 0.040 3 62495388 intron variant C/T snv 0.73 4
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs797045050
KIF1A
0.807 0.120 2 240797715 missense variant C/T snv 4
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs11787216 1.000 0.040 8 141605122 intron variant C/T snv 0.26 2
rs121912562
NR3C2
0.925 0.160 4 148435252 stop gained G/A;C snv 4.0E-06 2
rs121917893
NLGN3
0.807 0.160 X 71167508 missense variant C/T snv 2
rs121918799
SCN1A-AS1 ; SCN1A ; LOC102724058
0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 2
rs13294439 1.000 0.040 9 23358877 intron variant A/C snv 0.32 2
rs1553518509
MBD5
1.000 0.040 2 148468916 stop gained C/T snv 2
rs2230365
NFKBIL1
0.925 0.160 6 31557671 synonymous variant C/T snv 0.16 0.13 2
rs2898883
PHB
1.000 0.040 17 49405591 intron variant G/A snv 0.23 2
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 2