Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3774937
NFKB1
0.776 0.280 4 102513096 intron variant T/C snv 0.26 9
rs11928865
GRM7
1.000 0.120 3 7114015 intron variant T/A;G snv 2
rs11920109
GRM7
1.000 0.120 3 7170999 intron variant T/C snv 0.35 1
rs4648011
NFKB1
1.000 0.120 4 102554287 intron variant G/T snv 0.61 1
rs104894396
GJB2
0.672 0.400 13 20189511 stop gained C/T snv 5.8E-04 1.1E-04 28
rs765379963
TMCO1
0.701 0.520 1 165743172 stop gained G/A snv 1.2E-05 2.1E-05 19
rs771409809
WFS1
0.732 0.480 4 6301794 stop gained C/T snv 6.0E-05 7.0E-06 19
rs1135401743
HAAO ; MTA3
0.776 0.320 2 42769785 stop gained C/A;T snv 4.0E-06 11
rs104895564
NLRP12
0.925 0.200 19 53810809 stop gained G/A snv 1.5E-04 4.3E-04 3
rs121908361
SLC26A4
0.882 0.160 7 107689156 stop gained A/G;T snv 3
rs1302739538
GJB2
0.882 0.120 13 20189066 stop gained C/G;T snv 3
rs144948296
STRC ; CKMT1B
0.925 0.120 15 43604750 stop gained G/A;C snv 1.8E-04 3
rs397514588
OTOGL
0.925 0.120 12 80229341 stop gained C/T snv 3.8E-05 2.8E-05 2
rs397516875
GJB2
0.925 0.120 13 20189197 stop gained C/A;T snv 6.4E-05 2
rs549556142
CDC14A
0.925 0.120 1 100484347 stop gained C/A;T snv 1.6E-04; 4.1E-06 2
rs794726869
MARS2
0.925 0.120 2 197705955 stop gained C/T snv 7.0E-06 2
rs876657776
DIAPH1
0.925 0.160 5 141524167 stop gained G/A snv 2
rs876661408
CDC14A
0.925 0.120 1 100484440 stop gained C/T snv 4.3E-06 2
rs61753219
PEX6
0.672 0.400 6 42978330 missense variant G/A snv 3.6E-05 2.8E-05 64
rs4647924
FGFR3
0.600 0.520 4 1801844 missense variant C/A;G;T snv 4.2E-06; 4.2E-06 49
rs752298579
TANGO2
0.701 0.480 22 20061538 missense variant G/A snv 1.4E-04 7.0E-06 48
rs113994097
POLG
0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04 22
rs1558939623
CHN1
0.732 0.480 2 174824479 missense variant C/T snv 19
rs72474224
GJB2
0.708 0.440 13 20189473 missense variant C/A;T snv 7.7E-03 18
rs1318358361
ARID1B
0.724 0.240 6 156778678 missense variant C/G snv 2.1E-05 13