Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs762292772
SHANK3
0.882 0.160 22 50721505 frameshift variant G/-;GG delins 4
rs1555226315
TBX5
0.925 0.120 12 114398639 stop gained C/T snv 4
rs870142
STX18-AS1
0.851 0.120 4 4646320 intron variant C/G;T snv 2
rs769236847
CZ1P-ASNS ; ASNS
0.807 0.200 7 97869011 missense variant C/T snv 4.0E-06 3.5E-05 1
rs16835979
STX18-AS1
0.851 0.120 4 4633549 intron variant C/A snv 0.20 1
rs6824295
STX18-AS1
0.851 0.120 4 4612553 intron variant C/T snv 0.20 1
rs1800692
TNFRSF1A
0.925 0.120 12 6333180 missense variant A/G snv 0.64 0.71 1
rs1114167356
TPM1
1.000 0.080 15 63062261 missense variant C/T snv 1