Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1010184002
PEX6
0.689 0.400 6 42978878 stop gained C/T snv 7.0E-06 60
rs1014959895
PRMT7
0.763 0.360 16 68329105 stop gained G/C;T snv 4.0E-06; 1.6E-05 16
rs1057518848
TCF4
0.827 0.240 18 55229003 frameshift variant -/ATTG delins 15
rs1057518934
HERC2
0.851 0.240 15 28211095 frameshift variant G/- delins 8
rs1057518950
TPO
0.851 0.280 2 1484815 missense variant C/T snv 7
rs1057521721
GRIA3
0.851 0.200 X 123428020 missense variant G/A snv 5
rs112795301
FOXP1
0.776 0.160 3 70972634 stop gained G/A snv 13
rs1131692231
CYFIP2
0.827 0.280 5 157294834 missense variant C/T snv 13
rs1131692272
AFF3
0.851 0.240 2 100006808 missense variant C/T snv 9
rs1135401761
AHDC1
0.925 0.200 1 27548302 stop gained G/A;C snv 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1223073957
MED25
0.827 0.240 19 49835897 frameshift variant C/- delins 1.2E-05 1.4E-05 12
rs122445099
ATRX
0.827 0.400 X 77520832 stop gained G/A snv 6
rs1251713297
PRMT7
0.776 0.360 16 68355785 stop gained C/A snv 8.1E-06 15
rs1325394060
HUWE1
0.851 0.320 X 53534144 missense variant C/G;T snv 9.5E-06 9
rs1553630279
CTNNB1
0.807 0.160 3 41225049 stop gained C/T snv 7
rs1553655558
TRIP12
0.752 0.360 2 229830831 frameshift variant A/- delins 43
rs1554041295
ZSWIM6
0.925 0.160 5 61541917 stop gained C/T snv 2
rs1554150607
MEF2C
0.925 0.160 5 88823786 start lost C/G snv 2
rs1554691658
PTCH1
0.807 0.240 9 95459653 frameshift variant C/GGGTCCACAACATCT delins 11
rs1555103652
GRIN2B
0.882 0.240 12 13569973 missense variant A/C snv 11
rs1555321402
FOXG1
0.925 0.240 14 28768345 frameshift variant T/- delins 3
rs1555954284
DDX3X
0.752 0.360 X 41346607 missense variant C/T snv 24
rs1556024875
THOC2
0.882 0.160 X 123634002 missense variant G/A snv 4
rs1556910184
HUWE1
0.882 0.240 X 53534615 missense variant C/G snv 4