Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2371108
EOMES
1.000 0.080 3 27715527 downstream gene variant G/T snv 0.42 2
rs2412973
HORMAD2
1.000 0.080 22 30133642 intron variant C/A snv 0.54 2
rs2688608 1.000 0.080 10 73898591 regulatory region variant G/T snv 0.44 2
rs290986
SYK
1.000 0.080 9 90801254 upstream gene variant A/G snv 0.18 2
rs305217
PKN2
1.000 0.080 1 88754789 intron variant G/A snv 8.6E-02 2
rs307896
SAE1
1.000 0.080 19 47158236 intron variant G/A;C snv 2
rs3130000
DHX16
1.000 0.080 6 30660305 non coding transcript exon variant A/G;T snv 2
rs338610
LINC01967
1.000 0.080 3 28039951 intron variant A/G snv 0.73 2
rs35967351
SLAMF7
1.000 0.080 1 160742014 intron variant A/T snv 0.26 2
rs368243788
EIF2B4 ; SNX17
1.000 0.080 2 27368724 missense variant C/A;T snv 4.0E-06; 2.0E-04 2
rs3809263
NINJ2
1.000 0.080 12 664290 upstream gene variant C/T snv 0.33 2
rs394199
LINC00336 ; GGNBP1
1.000 0.080 6 33585803 intron variant C/T snv 0.43 2
rs4285028
SLC15A2
1.000 0.080 3 121941817 3 prime UTR variant A/C;G snv 2
rs4713429
HCG22
1.000 0.080 6 31053240 upstream gene variant C/G snv 0.20 2
rs479333
NLRC4
1.000 0.080 2 32264089 intron variant C/G;T snv 2
rs4798571
PTPRM
1.000 0.080 18 7584296 intron variant G/A snv 0.39 2
rs630923
CXCR5
1.000 0.080 11 118883644 upstream gene variant C/A snv 0.13 2
rs6880778 1.000 0.080 5 40398994 intergenic variant A/G snv 0.58 2
rs7255066
LOC107985305 ; PVR
1.000 0.080 19 44642803 intron variant T/C snv 0.43 2
rs7538427
GTF2B
1.000 0.080 1 88873739 intron variant C/T snv 0.93 2
rs7607490 1.000 0.080 2 12710994 intron variant G/A snv 0.13 2
rs771767 1.000 0.080 3 102029794 regulatory region variant A/G snv 0.70 2
rs874628
MPV17L2
1.000 0.080 19 18193890 missense variant A/G;T snv 0.24; 4.0E-06 2
rs9260489
HLA-A
1.000 0.080 6 29952555 upstream gene variant T/A;G snv 2
rs9262615
HCG22
1.000 0.080 6 31053384 upstream gene variant C/G snv 0.21 2