Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1569151872
TSPEAR-AS1 ; TSPEAR
0.851 0.240 21 44509225 frameshift variant GAC/AA delins 14
rs139455627
TSPEAR
0.851 0.240 21 44531087 stop gained G/A snv 3.2E-04 2.7E-04 14
rs113994152
TSEN54
0.790 0.160 17 75522000 missense variant G/T snv 9.0E-04 9.0E-04 11
rs796052243
SPATA5
0.695 0.520 4 122934574 inframe deletion CAA/- delins 54
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs28363170
SLC6A3
0.827 0.120 5 1393745 3 prime UTR variant -/AGTGGGGGCCCTGCATGCGTCCTGGGGTAGTACACGCTCC delins 8.1E-06 7
rs393795
SLC6A3
0.851 0.160 5 1428399 intron variant G/T snv 0.28 4
rs628031
SLC22A1
0.807 0.280 6 160139813 missense variant A/C;G snv 5.3E-05; 0.63 8
rs146539065
SEPSECS
0.752 0.240 4 25145092 synonymous variant C/T snv 2.8E-05 4.2E-05 34
rs776969714
SEPSECS
0.752 0.240 4 25145129 splice acceptor variant -/C delins 4.2E-05 34
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs2293054
NOS1
0.925 0.080 12 117263909 synonymous variant A/G;T snv 0.69; 4.0E-06 2
rs752513525
NDUFA13
0.882 0.120 19 19526257 missense variant G/A;T snv 2.4E-05 3
rs4911871
MIR1911 ; LOC105373313 ; HTR2C
1.000 0.080 X 114762580 intron variant A/G snv 0.15 1
rs1799836
MAOB
0.790 0.160 X 43768752 intron variant T/A;C snv 0.43 7
rs34778348
LRRK2 ; LOC105369736
0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04 15
rs34637584
LRRK2
0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs35801418
LRRK2
0.827 0.120 12 40321114 missense variant A/G snv 7
rs387907128
LOC112268170 ; PRRT2
0.925 0.080 16 29813850 missense variant C/T snv 4.0E-06 7.0E-06 2
rs56984562
LMNA
0.827 0.200 1 156137666 missense variant C/A;G;T snv 6
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1345423
GRIN2A
1.000 0.080 16 10154207 intron variant G/A;C;T snv 1