Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2270954
DCC ; LINC01917
1.000 0.040 18 53530928 3 prime UTR variant A/C snv 0.84 1
rs3916972
LOC105370345
1.000 0.040 13 105594285 intergenic variant A/C snv 0.51 1
rs4129585
TSNARE1 ; LOC107986983
1.000 0.040 8 142231572 intron variant A/C snv 0.68 1
rs4935752
GRIK4 ; LOC105369532
1.000 0.040 11 120818410 intron variant A/C snv 0.29 1
rs60266355 1.000 0.040 6 132648592 upstream gene variant A/C snv 6.1E-02 1
rs643410
TMEM245
1.000 0.040 9 109037283 intron variant A/C snv 0.93 1
rs746969672
DISC1 ; TSNAX-DISC1
1.000 0.040 1 232008917 missense variant A/C snv 4.0E-06 1
rs756656 1.000 0.040 22 19592662 regulatory region variant A/C snv 0.64 1
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 1
rs965041152
ADRA1A
1.000 0.040 8 26748580 3 prime UTR variant A/C snv 1.4E-05 1
rs14259
PSMD9
0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs6691840
GRIK3
0.827 0.120 1 36859876 missense variant A/C;G snv 0.27; 9.2E-05 5
rs2287939
AMACR ; C1QTNF3-AMACR
0.851 0.160 5 33998778 missense variant A/C;G snv 1.6E-05; 0.70 4
rs878567
HTR1A
0.882 0.040 5 63960164 intron variant A/C;G snv 4
rs2074898
NDUFS7
1.000 0.040 19 1391362 intron variant A/C;G snv 3
rs2292305
THBS1 ; FSIP1
0.882 0.080 15 39588621 missense variant A/C;G snv 4.0E-06; 0.16 3
rs3741775
DAO
0.925 0.080 12 108889827 intron variant A/C;G snv 3
rs6883197
CMYA5
0.882 0.040 5 79695550 intron variant A/C;G snv 3
rs963968092
EDNRA
0.882 0.120 4 147485844 missense variant A/C;G snv 8.0E-06 3
rs9960767
TCF4
0.925 0.040 18 55487771 intron variant A/C;G snv 3
rs420259
PALB2
0.925 0.040 16 23622705 intron variant A/C;G snv 2
rs10082463
SLC18A2
1.000 0.040 10 117261896 intron variant A/C;G snv 1
rs11038167
TSPAN18
1.000 0.040 11 44821583 intron variant A/C;G snv 1
rs1142636
SYN1
1.000 0.040 X 47606962 missense variant A/C;G snv 0.37 1
rs1558852
NRXN1
1.000 0.040 2 51024999 intron variant A/C;G snv 0.23 1