Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2660852 12 96051770 intergenic variant C/A snv 0.34 3
rs1052667
ARHGAP35
0.882 0.040 19 47004177 3 prime UTR variant C/G;T snv 6
rs730882002
TP53
0.925 0.040 17 7674956 missense variant T/C snv 6
rs1553260624
H3-3A
0.763 0.080 1 226064454 missense variant G/A snv 14
rs1458974438
STK11
0.807 0.080 19 1206957 missense variant G/A snv 9
rs1131691036
TP53
0.851 0.080 17 7675207 frameshift variant GCA/CC delins 8
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs11902171
ITGAV
0.925 0.080 2 186678500 3 prime UTR variant G/C snv 0.22 6
rs2269772
ITGA3
0.925 0.080 17 50072022 synonymous variant C/T snv 0.17 0.19 6
rs60745952
LOC107986195 ; LOC105377481
0.925 0.080 4 148827842 intron variant T/C snv 0.13 6
rs768827923
PIK3CD
0.851 0.080 1 9721816 missense variant T/G snv 6
rs10817938
PTCSC2
0.882 0.080 9 97700127 non coding transcript exon variant T/C snv 3.2E-02 5
rs16940
BRCA1
0.882 0.080 17 43093220 synonymous variant A/G snv 0.35 0.29 5
rs767151455
ERBB2
0.925 0.080 17 39708379 missense variant C/T snv 8.0E-06 4
rs12881063
LOC107984671 ; LOC105370397
1.000 0.080 14 20788017 downstream gene variant G/C snv 7.4E-02 3
rs1340026226
AR
1.000 0.080 X 67711662 missense variant G/A snv 9.5E-06 3
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv 16
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv 10
rs121913512
KIT
0.851 0.120 4 54728055 missense variant A/C;G snv 9
rs746429
SIPA1
0.882 0.120 11 65649963 synonymous variant G/A snv 0.31 0.30 8
rs771386507
HLA-B ; MIR6891
0.882 0.120 6 31355479 missense variant C/T snv 4.0E-06 6
rs2064863
AURKA
0.925 0.120 20 56387716 intron variant T/A;C;G snv 4
rs2835931
KCNJ6
1.000 0.120 21 37749345 intron variant C/A;T snv 4
rs477145
TIAM1
1.000 0.120 21 31390097 intron variant C/A;T snv 4
rs1040411
ATG5
1.000 0.120 6 106150148 intron variant G/A snv 0.47 3