Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 6
rs17689918
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
0.851 0.080 17 45832722 intron variant G/A snv 0.15 6
rs1864325
MAPT
0.882 0.160 17 45900461 intron variant C/T snv 0.14 6
rs1870293
SETD1A
0.827 0.120 16 30959620 intron variant T/C snv 0.62 6
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6
rs4129767
PGS1
17 78407903 intron variant G/A snv 0.46 6
rs4737010
ANK1
8 41772929 intron variant G/A snv 0.32 6
rs592423 6 139519556 intron variant A/C snv 0.50 6
rs605066 6 139508529 intron variant C/T snv 0.53 6
rs729761
LOC105375069 ; LOC107986598
0.925 0.120 6 43836834 intron variant T/A;G snv 6
rs733655
TMPRSS6
0.827 0.240 22 37099011 intron variant T/C snv 0.28 6
rs9389268
HBS1L
1.000 0.080 6 135098493 intron variant A/G snv 0.24 6
rs9471643
PGC
0.882 0.080 6 41751177 intron variant G/C snv 0.19 6
rs10495928
PRKCE
2 46126027 intron variant A/G snv 0.36 5
rs11066320
PTPN11
0.925 0.120 12 112468611 intron variant A/G snv 0.70 5
rs11072566
NRG4
0.925 0.120 15 76001630 intron variant A/G snv 0.45 5
rs115810
TRIM38
0.925 0.120 6 25975655 intron variant G/A;C snv 5
rs11627485
FNTB ; CHURC1-FNTB ; MAX
14 65020976 intron variant T/C snv 0.36 5
rs1175550
SMIM1
1 3774964 intron variant A/G snv 0.31 5
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24 5
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 5
rs12661667
USP49
6 41824807 intron variant C/T snv 0.20 5
rs13008603
PRKCE
2 46128709 intron variant C/A snv 0.10 5