Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs121918075
TTR
0.752 0.280 18 31598632 missense variant A/G snv 15
rs121918098
TTR
0.807 0.200 18 31592939 missense variant A/G snv 7
rs2072136
OAS3
0.851 0.120 12 112961114 synonymous variant G/A;C snv 0.31; 4.0E-06 6
rs1732778 0.882 0.080 12 113019120 upstream gene variant G/A snv 0.22 5
rs946880677
FAP
0.882 0.080 2 162224488 missense variant T/C snv 4