Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4804833
MAP2K7
1.000 0.040 19 7905750 intron variant A/G;T snv 1
rs6502892
MIR22 ; MIR22HG
1.000 0.040 17 1714314 intron variant T/C;G snv 1
rs10454453
PDE4B
1.000 0.040 1 66206849 intron variant C/A snv 0.48 1
rs10415555
PEPD
1.000 0.040 19 33519283 intron variant A/G snv 0.19 1
rs860554
PKP1
1.000 0.040 1 201293304 intron variant C/G;T snv 1
rs16938184
PRDM11
1.000 0.040 11 45179068 intron variant G/A;C snv 1
rs11805657
RGS7
1.000 0.040 1 240955726 intron variant T/C snv 0.87 1
rs3816995
SDK2
1.000 0.040 17 73339121 intron variant G/A snv 0.40 1
rs4583306
SLC6A4
1.000 0.040 17 30211697 intron variant A/G snv 0.37 1
rs144783209
SMAD1
1.000 0.040 4 145482377 intron variant G/C;T snv 1
rs7788
SNAPC2
1.000 0.040 19 7923232 3 prime UTR variant T/C snv 0.28 1
rs8076112
TLCD2
1.000 0.040 17 1708905 intron variant A/C;G snv 0.15 1
rs11060369
TMEM132D
1.000 0.040 12 129475652 intron variant A/C snv 0.41 1
rs7309727
TMEM132D
1.000 0.040 12 129470814 intron variant T/C snv 0.75 1
rs4795942
TMEM132E
1.000 0.040 17 34584149 intron variant C/T snv 0.72 1
rs10879357
TPH2
1.000 0.040 12 72020783 intron variant A/G snv 0.59 1
rs1487275
TPH2
1.000 0.040 12 72016512 intron variant C/A snv 0.71 1
rs10894993 0.925 0.080 11 100627998 intergenic variant T/G snv 4.7E-02 2
rs11210604 0.925 0.080 1 42158001 downstream gene variant T/A;G snv 2
rs7688285 0.925 0.040 4 157047466 intergenic variant G/A snv 0.10 2
rs1799923
CCK
0.925 0.040 3 42264802 5 prime UTR variant A/G snv 0.82 2
rs1800855
CCKAR
0.925 0.120 4 26489495 intron variant A/G;T snv 0.27 2
rs17035816
GLRB
0.925 0.040 4 157167312 intron variant A/G snv 0.11 2
rs4076452
LINC02210-CRHR1
1.000 0.040 17 45778528 intron variant G/C snv 0.16 2
rs11946004
NPY5R
0.925 0.040 4 163351551 synonymous variant G/A;T snv 0.10; 4.0E-06 2