Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs153109
IL27
0.623 0.600 16 28507775 intron variant T/C snv 0.43 37
rs12921862
AXIN1
0.763 0.200 16 331927 intron variant C/A snv 0.18 10
rs7977932
LRRC43 ; IL31
0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs4758680
LRRC43
0.763 0.320 12 122170805 intron variant T/A;G snv 9
rs2781666
ARG1
0.790 0.280 6 131572419 intron variant G/T snv 0.45 8
rs6503691
STAT5B
0.827 0.200 17 42242072 intron variant C/T snv 0.26 5
rs9268402
TSBP1 ; TSBP1-AS1
0.827 0.200 6 32373576 intron variant G/A snv 0.45 5
rs11465817
IL23R
0.882 0.120 1 67255414 intron variant C/A;T snv 4
rs1739843
HSPB7
0.882 0.040 1 16016759 intron variant T/C snv 0.62 4
rs2306969
LOC101928844 ; FUT3
0.925 0.040 19 5851790 intron variant A/G snv 0.76 4
rs10927875
ZBTB17
1.000 0.040 1 15972817 intron variant C/T snv 0.29 3
rs1009977
LGALS3
1.000 0.040 14 55136284 intron variant T/G snv 0.48 2
rs177415
PSEN1
1.000 0.040 14 73211255 intron variant T/C;G snv 2
rs3729843
TNNT2
0.925 0.040 1 201367856 intron variant C/A;G;T snv 1.8E-04; 0.42 2
rs670957
ACTC1 ; LOC101928174
0.925 0.080 15 34797231 intron variant G/A snv 0.45 2
rs150793926
CACNB4
1.000 0.040 2 151924550 intron variant TA/-;TATA;TATATA delins 1
rs3740346
LDB3
1.000 0.040 10 86692112 intron variant G/C snv 0.19 0.14 1
rs4341082
MGAM
1.000 0.040 7 142060046 intron variant C/G;T snv 1
rs4468255
LDB3
1.000 0.040 10 86679248 intron variant G/A;C snv 1
rs56165849
LDB3
1.000 0.040 10 86681952 intron variant A/G snv 0.50 1
rs6556795
LOC105377703
1.000 0.040 5 165040486 intron variant A/G;T snv 1
rs6660685
HSPB7 ; CLCNKA
1.000 0.040 1 16020493 intron variant A/G snv 0.70 1
rs73920070
FUT3 ; LOC101928844
1.000 0.040 19 5851772 intron variant G/A snv 1.8E-02 1
rs1846594 0.925 0.120 3 113197356 intergenic variant G/A;T snv 2