Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs28936379
PSEN2
0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs77369218
GBA
0.807 0.160 1 155235726 missense variant T/A snv 7
rs75548401
GBA
0.882 0.160 1 155236246 missense variant G/A snv 5.9E-03 6.2E-03 6
rs1315695444
SELP
1.000 0.040 1 169611580 missense variant C/G snv 4.0E-06 1.4E-05 2
rs1245342105
SPTBN1
1.000 0.040 2 54622367 missense variant T/C snv 4.0E-06 2
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs5522
NR3C2
0.732 0.320 4 148436323 missense variant C/T snv 0.88 0.89 19
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs2344484 0.925 0.040 5 135540941 upstream gene variant A/G snv 0.47 3
rs1018381
DTNBP1
0.882 0.040 6 15656839 intron variant G/A snv 0.16 6
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2189814
GRM3
0.925 0.040 7 86702440 intron variant T/A;C snv 3
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs1108580
DBH
0.790 0.240 9 133639992 splice region variant A/G snv 0.45 0.54 9
rs10748842
NRG3
0.807 0.120 10 81889983 intron variant T/C snv 0.13 8
rs1329650
HECTD2-AS1
0.882 0.080 10 91588363 regulatory region variant G/A;T snv 6
rs6584400
NRG3
0.851 0.120 10 81896770 intron variant G/A snv 0.22 6
rs761715536
ADRA2A
1.000 0.040 10 111079092 stop gained G/A;T snv 6.4E-06; 1.3E-05 3
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