Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267608383
MECP2
1.000 0.200 X 154030643 frameshift variant TCGGGCTC/- delins 5.8E-06 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs180177035
BRAF
0.752 0.280 7 140801502 missense variant T/C snv 35
rs878854402
TBL1XR1
0.851 0.280 3 177033050 missense variant T/C snv 6
rs587776690
ATR
0.882 0.280 3 142556439 synonymous variant T/C snv 4
rs61748392
MECP2
0.925 0.200 X 154031418 missense variant T/C snv 3
rs887386390
L2HGDH
0.925 0.120 14 50283990 missense variant T/C snv 3
rs10410239
CC2D1A
1.000 0.200 19 13919876 synonymous variant T/C snv 0.27 0.38 2
rs1287153074
FOXP1
1.000 0.080 3 70977021 missense variant T/C snv 4.0E-06 7.0E-06 2
rs1445362103
ARHGEF7
1.000 0.040 13 111244248 missense variant T/C snv 1.2E-05 7.0E-06 2
rs1471281484
WAPL
1.000 0.200 10 86500266 missense variant T/C snv 4.0E-06 2
rs3758653
DRD4
1.000 0.200 11 636399 upstream gene variant T/C snv 0.20 2
rs6530893
TUSC3
1.000 0.200 8 15671068 intron variant T/C snv 0.14 2
rs6994908
TUSC3
1.000 0.200 8 15674943 intron variant T/C snv 0.32 2
rs745756308
HNMT ; LOC107985948
1.000 2 138013874 missense variant T/C snv 4.0E-06 2
rs74900327
SMN2
1.000 0.120 5 70049747 missense variant T/C snv 2
rs1171889657
HADHB
2 26273656 missense variant T/C snv 4.0E-06 1
rs151191437
LIMK2
22 31277081 missense variant T/C snv 1.1E-03 1.2E-03 1
rs4846049
C1orf167 ; MTHFR
0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 11
rs255012 1.000 0.200 7 41189487 regulatory region variant T/A;C snv 2
rs1554032789
NIPBL
0.925 0.160 5 37048547 missense variant T/A snv 13
rs121918523
PHF8
0.925 0.200 X 54016662 stop gained T/A snv 3
rs869312966
SCN8A
0.827 0.120 12 51806345 missense variant G/T snv 7
rs723744
TTR
0.925 0.200 18 31592513 intron variant G/T snv 0.38 3