Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1031034
PPP3CA
1.000 0.040 4 101302229 intron variant C/A snv 0.29 1
rs11940117
CLNK
0.925 0.040 4 10725083 intergenic variant C/G;T snv 2
rs16872571
CLNK
0.925 0.080 4 10725229 intergenic variant C/T snv 0.33 2
rs4946936
FOXO3
0.790 0.160 6 108682118 3 prime UTR variant T/A;C snv 8
rs4308124
MIR4435-2HG
1.000 0.040 2 111252909 intron variant T/C snv 0.44 1
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 6
rs4766578
ATXN2
0.851 0.200 12 111466567 intron variant T/A snv 0.66 8
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs2234663
IL1RN
0.716 0.480 2 113130529 intron variant ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC/-;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC delins 14
rs3814231
CASP7
1.000 0.040 10 113721259 intron variant C/T snv 0.23 1
rs12771452
CASP7
1.000 0.040 10 113728572 intron variant G/A snv 0.23 1
rs4353229
CASP7
0.807 0.160 10 113729830 3 prime UTR variant T/C snv 0.23 6
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs638893 0.882 0.080 11 118827828 intergenic variant G/A snv 0.79 4
rs523604
CXCR5
0.882 0.120 11 118885029 intron variant A/G snv 0.53 3
rs613791
CXCR5
0.925 0.040 11 118893342 intron variant C/T snv 0.34 2
rs148136154 1.000 0.040 3 119564621 intergenic variant T/C;G snv 1
rs59374417 0.925 0.040 3 119569567 intergenic variant A/C;T snv 2
rs10986311
NEK6
1.000 0.040 9 124309214 intron variant T/C snv 0.34 1
rs561079
FLI1
1.000 0.040 11 128762660 intron variant T/C snv 0.37 1