Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114580964
PRRC2A
1.000 0.160 6 31636736 missense variant C/A;T snv 3.4E-03 1.4E-03 1
rs11057864
SCARB1
0.925 0.160 12 124851404 intron variant C/A snv 6.5E-02 2
rs274068
SLC5A11
0.925 0.160 16 24887651 intron variant C/A snv 0.74 2
rs434082
SLC8A1
0.925 0.160 2 40257934 intron variant C/T snv 0.14 3
rs11893826
SLC8A1
0.925 0.160 2 40337507 intron variant G/A snv 0.27 2
rs11889341
STAT4
0.732 0.480 2 191079016 intron variant C/T snv 0.21 12
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 11
rs5744168
TLR5
0.701 0.480 1 223111858 stop gained G/A snv 5.3E-02 4.4E-02 18
rs352140
TLR9
0.630 0.680 3 52222681 synonymous variant C/A;G;T snv 2.0E-05; 0.49 42
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18
rs7848647
TNFSF15
0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 13
rs6478109
TNFSF15
0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 12
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs4958881
TNIP1
0.827 0.280 5 151070675 intron variant T/C snv 0.21 7