Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs10833
IL15
0.776 0.160 4 141733394 3 prime UTR variant T/A;C snv 10
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs236918
PCSK7
0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs2281135
PNPLA3
0.851 0.160 22 43936690 intron variant G/A snv 0.19 10
rs1053005
STAT3
0.763 0.360 17 42313892 3 prime UTR variant T/C snv 0.25 10
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs12583006
TNFSF13B
0.807 0.320 13 108285104 intron variant T/A snv 0.21 8
rs137852769
GAREM2 ; HADHA
0.827 0.280 2 26195184 missense variant C/G snv 1.2E-03 1.0E-03 7
rs1051861187
ABCB4
0.827 0.080 7 87409385 missense variant A/G snv 6
rs4074
CXCL1
0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs57749775
KRT8
0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 6
rs2289030
MIR492 ; KRT19P2
0.882 0.120 12 94834510 non coding transcript exon variant G/C snv 9.7E-02 6.3E-02 6
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5
rs5743314
TLR3
0.851 0.160 4 186079221 intron variant G/C;T snv 5
rs2070666
APOC3
0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs11465817
IL23R
0.882 0.120 1 67255414 intron variant C/A;T snv 4
rs80338707
LOC100130283 ; PMM2
0.925 0.080 16 8847775 missense variant G/A;C snv 6.8E-05; 4.0E-06 4
rs104894630
SCO1
0.882 0.120 17 10692805 missense variant G/A snv 4
rs587777220
SCO1
0.882 0.120 17 10692932 missense variant C/T snv 1.2E-05 7.0E-06 4
rs7254880
ZNF699
0.882 0.160 19 9298599 intron variant C/G snv 0.16 4
rs7248668 0.925 0.080 19 39253181 upstream gene variant G/A snv 0.16 3
rs11881222
IFNL3
0.925 0.080 19 39244283 intron variant A/G snv 0.30 3
rs35724
NR1H4
0.925 0.040 12 100561600 intron variant C/G snv 0.52 3