Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs779724499
ITGA5 ; LOC102724050
12 54411885 missense variant G/A snv 1
rs7795743
EGFR ; EGFR-AS1
7 55182437 non coding transcript exon variant G/A snv 0.56 1
rs77709286
RET
0.752 0.160 10 43114502 missense variant C/G snv 4.0E-06 12
rs776880789
PGR ; PGR-AS1
0.925 0.080 11 101128241 missense variant G/C;T snv 4.7E-06; 4.7E-06 4
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv 16
rs773895706
RASGRF1
0.925 0.080 15 79090236 missense variant G/A snv 4.2E-06 3
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs772893086
ADARB1
0.925 0.080 21 45176099 missense variant A/C;G;T snv 4.0E-06 4
rs772551056
SDHB
0.807 0.120 1 17044824 missense variant C/A;T snv 4.0E-06 9
rs77191406
TNFAIP3
0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs771386507
HLA-B ; MIR6891
0.882 0.120 6 31355479 missense variant C/T snv 4.0E-06 6
rs771308693
PTK2
8 140752306 missense variant G/A snv 3.2E-05 7.0E-06 2
rs769483475
CD44
0.925 0.080 11 35229231 missense variant G/A snv 8.0E-06 3
rs768949233
IAH1 ; ADAM17
0.851 0.040 2 9490466 missense variant G/C;T snv 4.0E-06 5
rs768827923
PIK3CD
0.851 0.080 1 9721816 missense variant T/G snv 6
rs767649
MIR155HG ; MIR155
0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs767151455
ERBB2
0.925 0.080 17 39708379 missense variant C/T snv 8.0E-06 4
rs766914563
LOC112268426 ; CXCR4
0.732 0.320 2 136115082 synonymous variant C/T snv 7.0E-06 16
rs7668666
TLR3
1.000 4 186080138 intron variant C/A;T snv 4
rs765431049
LOC105375401 ; GNGT1 ; TFPI2
0.925 0.040 7 93890271 missense variant C/T snv 1.6E-05 4
rs7646409
PIK3CA
0.882 0.040 3 179182405 intron variant T/C snv 0.26 4
rs76322625
MET
1.000 0.080 7 116798111 3 prime UTR variant C/A;T snv 3
rs763059810
CXCR4
0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs76262710
RET
0.724 0.280 10 43113648 missense variant T/A;C;G snv 4.0E-06; 4.0E-06 17