Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6311
HTR2A
0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs75634836
HTR2A
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06 11
rs7997012
HTR2A
0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs3125
HTR2A
0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv 4
rs6561334
HTR2A
13 46849989 intron variant G/A snv 6.4E-02 4
rs2296972
HTR2A-AS1 ; HTR2A
0.925 0.080 13 46854336 intron variant A/C snv 0.70 4
rs1805055
HTR2A
0.882 0.120 13 46895833 missense variant G/C;T snv 2.0E-05; 1.8E-02 3
rs594242
HTR2A
1.000 0.040 13 46883917 intron variant C/A;G snv 3
rs6305
HTR2A
0.882 0.040 13 46892487 synonymous variant G/A snv 1.8E-02 1.7E-02 3
rs1923884
HTR2A
1.000 0.120 13 46847701 intron variant C/T snv 0.12 2
rs9316235
HTR2A
13 46871568 intron variant G/A snv 0.19 2
rs1885884
HTR2A ; HTR2A-AS1
13 46856141 non coding transcript exon variant C/A;G;T snv 2
rs12584920
HTR2A
1.000 0.040 13 46890902 intron variant G/C;T snv 1
rs1328674
HTR2A
1.000 0.120 13 46867572 intron variant T/C;G snv 1
rs1475196
HTR2A
1.000 0.040 13 46881488 intron variant A/C snv 1.4E-03 1
rs17069005
HTR2A
1.000 0.080 13 46849983 intron variant A/G snv 0.11 1
rs1923885
HTR2A
1.000 0.040 13 46848951 intron variant T/C snv 0.43 1
rs1923886
HTR2A
13 46849156 intron variant C/T snv 0.64 1
rs1928040
HTR2A
1.000 0.040 13 46873101 intron variant G/A snv 0.49 1
rs2070040
HTR2A
13 46893491 intron variant G/A snv 0.37 1
rs2770292
HTR2A
1.000 0.040 13 46860971 intron variant C/G snv 0.18 1
rs3742278
HTR2A
1.000 0.040 13 46845442 intron variant A/G snv 0.19 1
rs6561333
HTR2A
1.000 0.080 13 46846177 intron variant T/C snv 0.60 1