Source: ALL
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 0.15 272
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs3842225
TOR1A
0.882 0.120 9 129813148 3 prime UTR variant C/- del 0.16 6
rs769617030
AGFG1
1.000 0.040 2 227491553 synonymous variant A/T snv 4.9E-06 2
rs1252185897
GNAL
1.000 18 11868596 stop gained C/T snv 4.0E-06 2
rs143888944
RAB12
1.000 0.040 18 8636322 missense variant A/G snv 3.3E-04 4.1E-04 2
rs149427020
RAB12
1.000 0.040 18 8636256 missense variant G/A snv 4.5E-04 1.7E-04 2
rs371288995
RAB12
1.000 0.040 18 8636278 missense variant G/A snv 5.6E-05 4.9E-05 2
rs533268185
TFRC
1.000 0.040 3 196068103 missense variant T/C snv 2.4E-05 2
rs770304347
TFRC
1.000 0.040 3 196062895 missense variant C/T snv 4.0E-06 2
rs1239936594
CIZ1
9 128180461 missense variant G/A snv 1.4E-05 1
rs2296793
TOR1A
9 129822779 synonymous variant G/A snv 0.22 0.23 1
rs529094238
TOR1A
9 129822640 missense variant C/T snv 7.2E-05 2.8E-05 1