Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5030437
TRAF6
11 36503205 intron variant A/G snv 0.78 1
rs218916 1.000 0.040 8 89688709 intron variant C/T snv 0.67 2
rs2287886
CD209
0.776 0.280 19 7747650 upstream gene variant A/G;T snv 0.66 9
rs160441 1.000 0.040 8 89644760 intron variant T/C snv 0.55 2
rs4969170
LOC101928674
0.752 0.440 17 78364457 intron variant A/C;G snv 0.54 11
rs10510050 10 118867050 intron variant A/G snv 0.52 1
rs4694362
DCK
4 71028147 intron variant C/T snv 0.49 1
rs1523127
NR1I2
0.925 0.040 3 119782192 5 prime UTR variant C/A snv 0.48 3
rs10759637
SLC31A1 ; CDC26
1.000 0.040 9 113262744 3 prime UTR variant A/C snv 0.47 2
rs1523130
NR1I2
3 119780660 5 prime UTR variant T/C snv 0.47 1
rs7694379 1.000 4 87265357 intron variant G/A snv 0.40 3
rs4737420
LYN
0.925 0.080 8 55895622 non coding transcript exon variant T/C snv 0.38 3
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs760370
SLC29A1
0.925 0.120 6 44233216 intron variant A/G snv 0.36 3
rs3814055
NR1I2
0.925 0.040 3 119781188 5 prime UTR variant C/T snv 0.35 4
rs1800890
IL19
0.658 0.400 1 206776020 intron variant A/T snv 0.32 29
rs1801265
DPYD
0.763 0.280 1 97883329 missense variant A/G snv 0.28 13
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs735239
CD209
0.851 0.240 19 7748382 upstream gene variant A/G snv 0.26 5
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs17824620
RPH3A
12 112663189 intron variant C/A snv 0.26 2
rs3786136
RPA1
17 1869979 intron variant G/A snv 0.24 1
rs2297630
CXCL12
0.827 0.160 10 44376100 intron variant G/A;T snv 0.21 6
rs7729269
MCC
0.925 0.040 5 113384697 intron variant T/C snv 0.17 3
rs9574547 13 80057282 intron variant C/A snv 0.17 1