Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs528732638
CHST9 ; AQP4-AS1
0.851 0.120 18 26940224 intron variant A/-;AA;AAA;AAAA delins 5
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs1881457
IL13 ; TH2LCRR
0.790 0.280 5 132656717 intron variant A/C snv 0.21 9
rs242941
MAPT-AS1 ; CRHR1 ; LINC02210-CRHR1
0.790 0.200 17 45815154 intron variant A/C snv 0.62 9
rs2522833
PCLO
0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 7
rs2619522
DTNBP1
0.827 0.080 6 15653418 intron variant A/C snv 0.26 6
rs7296288
DHH
0.851 0.080 12 49086185 upstream gene variant A/C snv 0.50 5
rs884344
GDNF ; GDNF-AS1
0.882 0.120 5 37824138 intron variant A/C snv 0.33 5
rs1935062
DAOA ; DAOA-AS1
0.882 0.080 13 105475787 intron variant A/C snv 0.32 3
rs2133450
GRM7
0.925 0.080 3 7294765 intron variant A/C snv 0.38 3
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs14259
PSMD9
0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs2072115
RAPGEF3
0.882 0.080 12 47751585 intron variant A/C;G snv 5
rs4713916
FKBP5
0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs7305115
TPH2
0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131