Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9976767
UBASH3A
0.882 0.200 21 42416281 intron variant A/G snv 0.45 3
rs9937837
ITGAM
1.000 0.080 16 31287618 intron variant T/G snv 0.40 1
rs9889107
SBK1
1.000 0.080 16 28295666 intron variant A/G snv 0.70 1
rs9888739
ITGAM
0.882 0.120 16 31301932 intron variant C/T snv 0.26 3
rs9852465
LOC107986092
1.000 0.080 3 58479456 intergenic variant A/G snv 0.44 1
rs983492
SLC15A4
1.000 0.080 12 128821576 intron variant C/T snv 0.68 1
rs9808753
IFNGR2
0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18 17
rs9782955
LYST
1.000 0.080 1 235876577 intron variant T/C snv 0.82 1
rs967005
ZKSCAN4
1.000 0.080 6 28242910 3 prime UTR variant C/T snv 0.21 1
rs9652601
CLEC16A
1.000 0.080 16 11080508 intron variant G/A snv 0.34 1
rs961616
MDGA2
1.000 0.080 14 47052286 intron variant T/C snv 0.32 1
rs960709
TNIP1
0.882 0.120 5 151081488 intron variant A/G;T snv 5
rs9603612
COG6
0.925 0.120 13 39760715 intron variant C/G snv 0.30 2
rs959989
SLC15A4
1.000 0.080 12 128808163 intron variant A/T snv 9.1E-02 1
rs958476
LOC107984410 ; BARX2
0.925 0.160 11 129451923 3 prime UTR variant T/A;G snv 2
rs9515692 1.000 0.080 13 90141725 intergenic variant C/T snv 0.35 1
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs9462027
UHRF1BP1
1.000 0.080 6 34829464 intron variant G/A snv 0.37 1
rs9398235
DDO
1.000 0.080 6 110410913 intron variant G/A snv 0.21 1
rs9394274
TCP11
1.000 0.080 6 35147134 intron variant A/C;G;T snv 1
rs9380069 1.000 0.080 6 28235522 downstream gene variant A/G snv 0.13 2
rs9380064 1.000 0.080 6 28175340 upstream gene variant A/G snv 0.11 1
rs9373839
ATG5
0.882 0.080 6 106207742 intron variant T/C snv 0.15 3
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 5
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62