Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs370667926
MED23
1.000 6 131603129 missense variant C/T snv 1.6E-05 1.4E-05 1
rs387906728
UBE2A
1.000 X 119574743 missense variant G/A snv 1
rs587777570
KIF5C
1.000 2 148947018 missense variant G/A snv 1
rs745756308
HNMT ; LOC107985948
1.000 2 138013874 missense variant T/C snv 4.0E-06 1
rs758252808
HNMT
1.000 2 137970206 missense variant G/A snv 4.1E-06 1
rs864309721
CDC42
1.000 1 22086451 missense variant A/G snv 1
rs587777308
GABRA1
0.763 0.040 5 161873196 missense variant G/A snv 8
rs398122368
SMARCB1
0.925 0.040 22 23791772 missense variant G/A;C snv 1
rs672601376
LOC105369668 ; GRIN2B
0.925 0.040 12 13608760 missense variant A/C snv 1
rs672601378
GRIN2B ; LOC105369668
0.882 0.040 12 13615149 missense variant C/T snv 1
rs869320632
LMAN2L
0.925 0.040 2 96739883 missense variant C/T snv 1
rs774843232
PGAP2
0.851 0.080 11 3825024 missense variant G/A;C;T snv 8.0E-06; 3.6E-05; 1.2E-05 8
rs142698837
TG
0.851 0.080 8 132869781 missense variant G/A snv 7.6E-04 7.0E-04 5
rs61751444
MECP2
0.882 0.080 X 154030903 missense variant G/A snv 4
rs730882213
ADAT3 ; SCAMP4
0.925 0.080 19 1912477 missense variant G/A snv 7.0E-06 3
rs1057516085
KCNQ2
0.827 0.080 20 63444747 missense variant C/T snv 2
rs61751367
MECP2
0.925 0.080 X 154030939 stop gained G/A snv 2
rs121434612
PAK3
1.000 0.080 X 111142119 missense variant C/T snv 1
rs121917899
PQBP1
1.000 0.080 X 48901944 missense variant A/G snv 1
rs281860639
MIR6894 ; KDM5C
1.000 0.080 X 53199048 stop gained G/T snv 1
rs398122917
CLIC2
0.882 0.080 X 155280059 missense variant G/C snv 4.4E-05 1.1E-04 1
rs786201003
NALCN
0.925 0.080 13 101083752 missense variant C/T snv 1
rs587777623
DEAF1
0.882 0.120 11 686986 missense variant G/A snv 4.0E-06 5
rs1057519087
MFSD2A
0.925 0.120 1 39967632 missense variant C/T snv 7.0E-06 1
rs1131692042
RPL10 ; SNORA70
0.925 0.120 X 154399803 missense variant C/T snv 1