Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1519480
BDNF-AS
0.925 0.040 11 27654165 intron variant C/T snv 0.54 4
rs1556995
GRIK2
1.000 0.040 6 101869470 intron variant C/A;T snv 1
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs16965628
SLC6A4
0.882 0.040 17 30228407 intron variant G/C snv 0.14 3
rs17162912 1.000 0.040 1 222801584 intergenic variant T/C snv 0.11 1
rs1755715
GPR135
1.000 0.040 14 59440374 intron variant A/T snv 0.55 1
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1799972
OPRM1
0.827 0.080 6 154039561 missense variant C/A;G;T snv 4.1E-06; 1.7E-02 6
rs1800042
HTR1A
1.000 0.040 5 63960902 missense variant C/A;T snv 8.0E-06; 1.4E-03 2
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1805477
GRIN2B
0.882 0.080 12 13561795 3 prime UTR variant T/A;C;G snv 3
rs1838733
PDE4D
1.000 0.040 5 59237566 intron variant C/T snv 0.32 1
rs2000292
LOC105377864
1.000 0.040 6 77457228 downstream gene variant G/A snv 0.31 1
rs201333291
CDH2
1.000 0.040 18 27985092 missense variant T/C snv 4.0E-06 1.4E-05 1
rs2071592
ATP6V1G2-DDX39B ; ATP6V1G2 ; NFKBIL1
0.882 0.200 6 31547563 intron variant T/A;C snv 3
rs2075507
COMT ; TXNRD2
0.925 0.040 22 19940569 intron variant G/A;T snv 2
rs2097063 1.000 0.040 18 73963859 intron variant T/C snv 0.19 1
rs2097603
TXNRD2 ; COMT
0.882 0.040 22 19940569 intron variant G/A;T snv 3
rs2228622
SLC1A1 ; SPATA6L
1.000 0.040 9 4564432 synonymous variant G/A snv 0.39 0.35 1
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs2268490
CAV3 ; OXTR
1.000 0.040 3 8755399 intron variant C/T snv 0.18 2
rs2268493
CAV3 ; OXTR
0.882 0.040 3 8759154 intron variant T/C snv 0.25 3
rs2289664
CDH2
0.925 0.120 18 27952340 missense variant T/C snv 2.5E-02 2.0E-02 2
rs2364841
ADCK1
1.000 0.040 14 77817693 intron variant A/G snv 0.86 1
rs2378672
NTRK2
1.000 0.040 9 85016119 intron variant C/T snv 0.93 1