Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs6505162
NSRP1 ; MIR3184 ; MIR423
0.695 0.320 17 30117165 5 prime UTR variant A/C;T snv 0.50; 3.1E-05 25
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1137100
LEPR
0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs187084
TLR9
0.641 0.480 3 52227015 intron variant A/G snv 0.38 36
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs4804803
CD209
0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
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
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5
rs11881222
IFNL3
0.925 0.080 19 39244283 intron variant A/G snv 0.30 3
rs2294918
PNPLA3
0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70 3
rs1281032650
LNPEP
5 96979168 missense variant A/G snv 1
rs2071025
COL11A2
6 33175979 intron variant A/G snv 0.28 0.29 1
rs231775
CTLA4
0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs57749775
KRT8
0.851 0.080 12 52904822 missense variant A/G;T snv 1.7E-03; 4.0E-06 6
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs11554495
KRT8
0.701 0.240 12 52904798 missense variant C/A snv 4.9E-03 5.4E-03 19
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11