Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7512552
MRPS21 ; LOC105371434
1.000 0.120 1 150293284 upstream gene variant T/C snv 0.63 4
rs174448 1.000 0.120 11 61872101 downstream gene variant G/A snv 0.61 3
rs3917265
IL1R1
1.000 0.120 2 102162001 intron variant T/C snv 0.50 2
rs7127307 1.000 0.120 11 128317488 regulatory region variant T/C snv 0.47 2
rs10067777
TMEM232
1.000 0.120 5 110490595 intron variant A/G snv 7.4E-02 1
rs10199605
LINC00299
1.000 0.120 2 8354967 intron variant G/A snv 0.26 1
rs10214237 1.000 0.120 5 35883632 downstream gene variant T/C snv 0.21 1
rs10738626 1.000 0.120 9 22373458 intergenic variant C/G;T snv 1
rs10888499 1.000 0.120 1 152560266 intergenic variant C/A;T snv 1
rs10995251
LOC105378327 ; ZNF365
1.000 0.120 10 62638706 intron variant C/T snv 0.29 1
rs11205006 1.000 0.120 1 152467700 intergenic variant A/T snv 0.72 1
rs12144049 1.000 0.120 1 152468434 intergenic variant C/G;T snv 1
rs12188917
TH2LCRR ; IL13
1.000 0.120 5 132655393 intron variant T/C;G snv 1
rs1444418 1.000 0.120 10 62800710 intron variant A/G snv 0.22 1
rs148203517
HLA-B ; MIR6891
1.000 0.120 6 31356323 missense variant G/A;T snv 1
rs1665050
RNF111
1.000 0.120 15 59001406 intron variant A/G;T snv 1
rs16999165 1.000 0.120 20 54190682 intergenic variant A/G snv 5.5E-02 1
rs17006471
CD207
1.000 0.120 2 70841493 intergenic variant T/C snv 0.42 1
rs17173197
PRKAG2
1.000 0.120 7 151571834 non coding transcript exon variant C/T snv 0.34 1
rs17881320
STAT3
1.000 0.120 17 42333221 intron variant G/A;T snv 6.0E-02 1
rs2041733
CLEC16A ; LOC105371081
1.000 0.120 16 11135732 intron variant T/C;G snv 1
rs2143950
FAM177A1 ; PPP2R3C ; LOC101927178
1.000 0.120 14 35103151 intron variant C/T snv 0.17 1
rs2212434 1.000 0.120 11 76570549 intergenic variant C/T snv 0.39 1
rs2271404
MIR4435-2HG
1.000 0.120 2 111246290 non coding transcript exon variant T/C snv 0.12 1
rs2393903
ZNF365
1.000 0.120 10 62620576 intron variant T/A;C snv 1