Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143046984
LOC105370557 ; PCNX1
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02 9
rs6147150
ERBB4
0.827 0.160 2 211380365 3 prime UTR variant -/AAAATAGGATTG delins 5
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs202110856
ERAP1
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05 9
rs771306418
CAMK1 ; OGG1
0.851 0.120 3 9765885 splice acceptor variant -/C delins 5
rs587780078
MUTYH
0.882 0.120 1 45331514 frameshift variant -/CC delins 1.6E-04 2.7E-04 4
rs28360317
XRCC4
0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs1567755946
AXIN2
0.925 0.080 17 65537563 frameshift variant -/CGCGGGAGGCAGC delins 2
rs863223400
CERNA3 ; RPS20 ; SNORD54
1.000 0.080 8 56073724 frameshift variant -/T delins 1
rs377429877
STARD13
0.776 0.080 13 33518027 intron variant -/TAA delins 6.0E-02 10
rs10680577
RAB4B-EGLN2 ; EGLN2
0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs70991108
MSH3 ; DHFR
0.807 0.280 5 80654344 intron variant -/TCGCGCGTCCCGCCCAGGT;TGGCGCGTCCCGCCCAGGT ins 0.51 6
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs587776642
BUB1
1.000 0.080 2 110638153 frameshift variant A/- del 1
rs587776687
PPARG
1.000 0.080 3 12392683 frameshift variant A/- delins 1
rs61764370
KRAS
0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs712
KRAS
0.677 0.360 12 25209618 3 prime UTR variant A/C snv 0.46 24
rs2069762
IL2
0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 23
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs735482
CD3EAP ; ERCC1
0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs6058093
PIGU
0.776 0.080 20 34625392 intron variant A/C snv 0.55 12
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 11
rs7763881
HULC ; LOC100506207
0.776 0.160 6 8653014 non coding transcript exon variant A/C snv 0.44 11
rs1566734
PTPRJ
0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 10
rs9924886
CDH3
0.776 0.080 16 68710036 intron variant A/C snv 0.25 10