Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs587778967
EPM2AIP1 ; MLH1
0.925 0.200 3 36993548 start lost A/C;G snv 8
rs876658923
EPM2AIP1 ; MLH1
1.000 0.120 3 36993593 frameshift variant TGAACCG/- delins 3
rs372043866
ERBB2
0.732 0.240 17 39727965 missense variant G/A;C;T snv 3.2E-05; 2.4E-05; 1.2E-05 18
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs2077647
ESR1
0.732 0.320 6 151807942 synonymous variant T/A;C snv 8.1E-06; 0.46 16
rs3798577
ESR1
0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 9
rs188957694
ESR1
0.882 0.080 6 151944218 missense variant G/A;C snv 4.0E-05 4.9E-05 6
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 16
rs121913482
FGFR3
0.630 0.680 4 1801837 missense variant C/T snv 45
rs121913483
FGFR3
0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
rs78311289
FGFR3
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs121913485
FGFR3
0.716 0.400 4 1804372 missense variant A/G snv 18
rs28931615
FGFR3
0.732 0.240 4 1804426 missense variant C/A;T snv 13
rs121913484
FGFR3
0.851 0.240 4 1804365 missense variant A/T snv 5
rs587779383
FGFR3
0.851 0.120 4 1806157 missense variant A/C;G;T snv 5
rs121913480
FGFR3
1.000 0.120 4 1806604 missense variant G/T snv 2
rs351855
FGFR4
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs1400966919
FGFR4
0.925 0.240 5 177096737 missense variant G/A snv 1.4E-05 3
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs758272654
GNAS
0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs917411291
GZMM
0.851 0.360 19 544072 start lost A/C;G snv 9
rs917570055
GZMM
0.882 0.360 19 547342 start lost A/G snv 7
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 37