Disease: Child Development Disorders, Pervasive
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs4129585
TSNARE1 ; LOC107986983
1.000 0.040 8 142231572 intron variant A/C snv 0.68 4
rs6704768
GIGYF2
1.000 0.040 2 232727791 intron variant G/A snv 0.54 4
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 4
rs10149470 1.000 0.040 14 103551616 upstream gene variant A/G snv 0.54 3
rs11740474
GALNT10
1.000 0.040 5 154301187 intron variant A/T snv 0.37 3
rs12552
OLFM4
1.000 0.040 13 53051646 3 prime UTR variant A/G snv 0.58 3
rs12704290
GRM3-AS1 ; GRM3
1.000 0.040 7 86798310 intron variant G/A snv 8.9E-02 3
rs12826178
SHMT2
1.000 0.040 12 57228588 upstream gene variant G/T snv 5.3E-02 3
rs133047
MRTFA
1.000 0.040 22 40631815 intron variant T/C snv 0.93 3
rs1620977
NEGR1
1.000 0.040 1 72263459 intron variant A/G;T snv 3
rs2007044
CACNA1C
0.882 0.040 12 2235794 intron variant A/G snv 0.50 3
rs4702
FES ; FURIN
1.000 0.040 15 90883330 3 prime UTR variant G/A;C snv 3
rs55661361
NRGN
1.000 0.040 11 124744061 intron variant G/A snv 0.43 3
rs62378245
MEF2C-AS1
1.000 0.040 5 89448145 intron variant C/T snv 0.25 3
rs6940116 1.000 0.040 6 27740953 upstream gene variant A/G snv 0.18 3
rs72986630
ZNF823
1.000 0.040 19 11738921 5 prime UTR variant C/A;T snv 3
rs7432375
STAG1
1.000 0.040 3 136569563 intron variant G/A snv 0.35 3
rs7746199
POM121L2
1.000 0.040 6 27293545 intron variant C/T snv 0.18 3
rs9607782
EP300-AS1
1.000 0.040 22 41191552 intron variant T/A snv 0.23 3
rs9636107
TCF4
1.000 0.040 18 55532886 intron variant A/G;T snv 3