Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16957920 1.000 0.040 13 87710848 intergenic variant G/C snv 6.4E-02 1
rs200754866
ABCB1
1.000 0.040 7 87536484 missense variant C/A;T snv 1.2E-05; 3.6E-05 1
rs966923314
ABCB1
1.000 0.040 7 87601026 5 prime UTR variant T/C snv 7.0E-06 1
rs17822471
ABCC11
1.000 0.040 16 48208468 missense variant G/A snv 5.1E-02 4.8E-02 1
rs763794263
ABCC8
1.000 0.040 11 17432232 missense variant G/A snv 6.3E-05 3.5E-05 1
rs931572188
ACAD8
1.000 0.040 11 134256593 missense variant C/A;G;T snv 4.0E-06 1
rs7574965
CROCC2 ; LOC112268440
1.000 0.040 2 240930976 synonymous variant C/A;T snv 2.8E-05; 6.7E-03 1
rs1218899764
DPYD
1.000 0.040 1 97515829 missense variant A/G snv 1
rs762392769
FLT3
1.000 0.040 13 28018553 missense variant C/T snv 8.0E-06 1
rs2228075
IMPDH1
1.000 0.040 7 128394575 synonymous variant C/A;G;T snv 0.27 1
rs1341929358
NR1I3 ; TOMM40L
1.000 0.040 1 161230905 missense variant A/G snv 4.0E-06 7.0E-06 1
rs586014
RAD18
1.000 0.040 3 8965408 upstream gene variant A/G snv 0.82 1
rs618784
RAD18
1.000 0.040 3 8962743 intron variant C/G;T snv 1
rs654448
RAD18
1.000 0.040 3 8893530 intron variant C/T snv 0.85 1
rs6763823
RAD18
1.000 0.040 3 8892799 intron variant G/A;T snv 0.18 1
rs9880051
RAD18
1.000 0.040 3 8962766 intron variant C/G;T snv 1
rs7320366
SUCLA2
1.000 0.040 13 47973332 missense variant A/G;T snv 8.0E-06; 0.75 1
rs7438135
UGT2B7
1.000 0.040 4 69095621 intron variant G/A snv 0.58 1
rs669884
XDH
1.000 0.040 2 31350126 missense variant G/A;C;T snv 4.7E-04 1
rs11719165 0.925 0.040 3 194865359 intergenic variant T/C snv 0.53 2
rs117829974 1.000 0.040 3 62886233 intergenic variant C/A;G;T snv 2
rs12046844 0.925 0.040 1 65772696 regulatory region variant G/A snv 0.17 2
rs1901440 0.925 0.040 2 133680388 intergenic variant C/A snv 0.58 2
rs2501846 1.000 0.040 1 212668592 upstream gene variant T/C snv 0.24 2
rs7091672 0.925 0.040 10 118836909 intron variant T/A;C;G snv 2