Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs781172058
CXCR4
0.732 0.320 2 136115340 synonymous variant C/T snv 4.0E-06 16
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 12
rs11225395
MMP8
0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv 11
rs3809865
THCAT158 ; ITGB3
0.790 0.240 17 47311220 3 prime UTR variant T/A;G snv 11
rs4671393
BCL11A
0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs3020449
ESR2
0.807 0.200 14 64306674 intron variant A/G;T snv 10
rs3741219
MRPL23 ; H19 ; HOTS
0.776 0.280 11 1995389 non coding transcript exon variant A/G snv 0.42 10
rs75873440
RET
0.763 0.200 10 43112173 missense variant G/A;T snv 4.4E-05 10
rs778036161
RUNX1T1
0.776 0.080 8 92017363 missense variant T/C snv 8.0E-06 9
rs10053538
HAVCR2
0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs10399805
CHI3L1
0.851 0.240 1 203186870 upstream gene variant G/A;T snv 7
rs10814325
RECK
0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7
rs12918952
WWOX
0.851 0.120 16 78386878 missense variant G/A;C;T snv 7
rs2228468
ACKR2 ; KRBOX1 ; CYP8B1
0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03 6
rs2622621
ABCG2
0.851 0.240 4 88109768 intron variant C/A;G snv 6
rs3829078
CA9
0.851 0.160 9 35679254 missense variant A/G;T snv 8.2E-02 6
rs4693608
HPSE
0.827 0.200 4 83320204 intron variant G/A;C snv 6
rs1143630
IL1B
0.827 0.160 2 112834078 intron variant T/A;G snv 5
rs767741751
MCPH1 ; ANGPT2
0.851 0.120 8 6562846 missense variant C/A snv 4.0E-06 5
rs770327175
CXCR4
0.851 0.120 2 136115878 missense variant C/A;T snv 8.0E-06 5