Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs1801270
CDKN1A
0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05 22
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs2267437
DESI1 ; XRCC6
0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs55832599
TP53
0.716 0.360 17 7673821 missense variant G/A snv 18
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs2233678
PIN1 ; LOC100996288
0.732 0.360 19 9834503 non coding transcript exon variant G/A;C snv 14
rs872071
IRF4
0.742 0.360 6 411064 3 prime UTR variant A/G;T snv 13
rs1131691003
TP53
0.752 0.360 17 7676381 splice donor variant C/A;G snv 12
rs1131691042
TP53
0.752 0.360 17 7675052 splice donor variant C/T snv 12
rs13347
CD44
0.763 0.320 11 35231725 3 prime UTR variant C/A;T snv 12
rs4754
SPP1
0.752 0.360 4 87981540 missense variant T/A;C snv 0.32 12
rs9138
SPP1
0.776 0.360 4 87983190 3 prime UTR variant A/C;T snv 12
rs3021097
IL10 ; IL19
0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs498872
PHLDB1
0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 10
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 9
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 9
rs9642880
CASC11
0.776 0.240 8 127705823 intron variant G/A;T snv 9
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 7
rs2075555
COL1A1
0.807 0.240 17 50196930 intron variant T/A;G snv 6
rs29230
GABBR1
0.807 0.440 6 29608616 missense variant A/C;G snv 4.1E-06; 0.18 6
rs12220909
MIR4293 ; FRMD4A
0.827 0.240 10 14383222 mature miRNA variant G/C;T snv 4.9E-03 5