Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 36
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 36
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 23
rs12203592
IRF4
0.649 0.320 6 396321 intron variant C/T snv 0.10 16
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 16
rs2242652
TERT
0.724 0.400 5 1279913 intron variant G/A snv 0.18 16
rs2234663
IL1RN
0.716 0.480 2 113130529 intron variant ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC/-;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC delins 14
rs4646536
CYP27B1
0.724 0.440 12 57764205 intron variant A/G snv 0.38 0.32 14
rs11225395
MMP8
0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs927650
CYP24A1
0.763 0.240 20 54156202 intron variant T/A;C snv 9
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50 8
rs2107301
VDR
0.807 0.120 12 47861787 intron variant G/A snv 0.26 7
rs12621278
ITGA6
0.790 0.280 2 172446825 intron variant A/G snv 4.9E-02 6
rs12913832
HERC2
0.763 0.200 15 28120472 intron variant A/G snv 0.50 6
rs10931936
CASP8
0.827 0.120 2 201279205 intron variant T/C snv 0.72 5
rs10951982
RAC1
0.851 0.160 7 6382925 intron variant G/A;T snv 5
rs10754833
NID1
0.851 0.040 1 236021631 intron variant T/A;C snv 4
rs16953002
FTO
0.882 0.080 16 54080912 intron variant G/A snv 0.19 4
rs4845618
IL6R
0.851 0.160 1 154427539 intron variant G/T snv 0.53 4
rs6465657
LMTK2
0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 4
rs10757257
MTAP
0.882 0.080 9 21806565 intron variant G/A snv 0.34 3
rs12418451
LOC338694 ; LOC105369366
0.882 0.080 11 69167951 intron variant G/A snv 0.22 3
rs13016963
FLACC1
0.851 0.080 2 201298088 intron variant A/G snv 0.59 3