Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs155417
DRD1
1.000 0.040 5 175441837 synonymous variant T/A;C snv 0.99 1
rs10747050
GRIN1
1.000 0.040 9 137161424 splice region variant G/A snv 0.94 0.95 1
rs450046
PRODH ; DGCR6
0.851 0.280 22 18913491 missense variant C/T snv 0.93 2.8E-03 2
rs385440
DGCR6 ; PRODH
1.000 0.040 22 18913577 3 prime UTR variant A/G snv 0.91 7.7E-05 1
rs2227956
HSPA1L
0.752 0.400 6 31810495 missense variant G/A;C;T snv 0.87 9
rs7758659
DTNBP1
1.000 0.040 6 15593009 intron variant T/A;C snv 5.2E-06; 0.82 1
rs3813535
STON2
1.000 0.040 14 81278392 missense variant A/C;G snv 4.0E-06; 0.81 1
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 18
rs1648833
JMJD7-PLA2G4B ; PLA2G4B
1.000 0.040 15 41842325 non coding transcript exon variant C/G;T snv 0.80 1
rs372055
DGCR6 ; PRODH
1.000 0.040 22 18913237 synonymous variant G/A snv 0.78 1
rs6971
TSPO
0.742 0.200 22 43162920 missense variant A/G snv 0.76 0.75 11
rs165815
ARVCF
0.882 0.120 22 19971950 missense variant C/T snv 0.75 0.72 5
rs2229113
IL10RA
0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs490460
BACE1 ; BACE1-AS
1.000 0.040 11 117293049 splice region variant C/A;T snv 0.74 1
rs2303579
NEDD4
0.925 0.040 15 55860531 missense variant T/C snv 0.74 0.72 2
rs7157599
DEGS2
0.925 0.040 14 100159565 missense variant C/T snv 0.73 0.76 3
rs1009382
TNXB
1.000 0.040 6 32058330 missense variant C/A;G;T snv 0.72 1
rs1045280
ARRB2
0.882 0.160 17 4719343 synonymous variant C/T snv 0.71 0.62 3
rs2230808
ABCA1
0.827 0.240 9 104800523 missense variant T/C snv 0.71 0.60 6
rs2307223
PAWR
0.925 0.040 12 79621127 missense variant A/C;T snv 0.10; 0.70 2
rs2287939
AMACR ; C1QTNF3-AMACR
0.851 0.160 5 33998778 missense variant A/C;G snv 1.6E-05; 0.70 4
rs2070565
DNMT3L
0.925 0.080 21 44261270 splice region variant T/C snv 0.70 0.75 3
rs2278008
C1QTNF3-AMACR ; AMACR
0.851 0.160 5 33989413 missense variant C/T snv 0.70 0.74 4
rs907094
PPP1R1B
1.000 0.040 17 39634118 intron variant G/A snv 0.69 0.60 1
rs204887
TNXB
1.000 0.040 6 32061449 stop gained A/G;T snv 0.69; 4.1E-06 1