Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1989969
VDR
0.827 0.120 12 47884227 intron variant A/C;G;T snv 0.60 8
rs4767364
NAA25
0.807 0.160 12 112083644 intron variant G/A snv 0.45 8
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17 7
rs2107301
VDR
0.807 0.120 12 47861787 intron variant G/A snv 0.26 7
rs3176352
CDKN1A
0.807 0.120 6 36684562 intron variant C/A;G;T snv 8.0E-06; 0.37; 2.0E-05 7
rs452204
IL1RN
0.807 0.200 2 113131484 intron variant G/A snv 0.45 7
rs9841504
ZBTB20
0.827 0.120 3 114643917 intron variant C/G;T snv 7
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 6
rs115510139
COL6A3
0.827 0.120 2 237331726 intron variant A/T snv 0.60 6
rs10509670
PLCE1
0.851 0.080 10 94308190 intron variant A/G snv 0.30 5
rs11066015
ACAD10
0.925 0.120 12 111730205 intron variant G/A snv 5.9E-03 5
rs12231737
TRAFD1
0.925 0.120 12 112136812 intron variant C/T snv 5.9E-03 5
rs13016963
FLACC1
0.851 0.080 2 201298088 intron variant A/G snv 0.59 5
rs1534891
CSNK1E ; TPTEP2-CSNK1E
0.827 0.200 22 38299094 intron variant T/C snv 0.90 5
rs2014300
RUNX1
0.851 0.080 21 34985564 intron variant A/G;T snv 0.75 5
rs31563 0.851 0.160 5 135899917 intron variant C/A;T snv 5
rs315919
IL1RN
0.851 0.120 2 113118636 intron variant T/G snv 0.55 5
rs3181052
IL1RN
0.851 0.120 2 113128472 intron variant G/A snv 0.16 5
rs7248488
ZNF208
0.851 0.160 19 22005907 intron variant A/C snv 0.59 5
rs6720283
COL6A3
0.882 0.120 2 237401239 intron variant G/A snv 0.31 4
rs738722
CHEK2
0.882 0.120 22 28734024 intron variant T/C snv 0.67 4
rs8103163
ZNF208
0.882 0.120 19 21991950 intron variant A/C snv 0.59 4
rs2320615
NAF1
0.925 0.080 4 163148797 intron variant A/G snv 0.78 3
rs312986 0.925 0.080 18 1898710 intron variant A/G;T snv 3
rs31564
IL9
0.925 0.080 5 135894564 intron variant G/A;T snv 3