Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7804372
CAV1
0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs3807987
CAV1
0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs1997623
CAV1
0.807 0.160 7 116525306 missense variant A/C;G snv 0.86 9
rs3807992
CAV1
0.925 0.080 7 116557191 intron variant G/A snv 0.28 5
rs12672038
CAV1
0.925 0.080 7 116547052 intron variant G/A snv 7.6E-02 4
rs3757733
CAV1
1.000 0.040 7 116553675 intron variant T/A snv 0.26 4
rs387906666
CBL
0.827 0.080 11 119278182 missense variant A/C;G snv 5
rs3116496
CD28
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 11
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 18
rs754944509
CNTNAP1
0.851 0.080 17 42690793 missense variant C/T snv 4.4E-05 4
rs796065343
CSF3R
0.776 0.080 1 36467833 missense variant G/A snv 12
rs1258094111
CTSG
0.925 0.040 14 24575388 missense variant C/T snv 4.0E-06 2
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs2228014
CXCR4
0.752 0.240 2 136115514 synonymous variant G/A snv 4.6E-02 3.5E-02 14
rs3745274
CYP2B6
0.672 0.480 19 41006936 missense variant G/A;T snv 4.0E-06; 0.27 30
rs869312828
DDX41 ; DOK3
0.807 0.080 5 177512369 missense variant C/T snv 7
rs1408538785
DNAH8
0.827 0.080 6 38761760 missense variant A/G snv 7.0E-06 6
rs387906553
ELANE
0.827 0.120 19 853022 missense variant G/A;C snv 1.2E-05 6
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs2077647
ESR1
0.732 0.320 6 151807942 synonymous variant T/A;C snv 8.1E-06; 0.46 16
rs2228480
ESR1
0.724 0.360 6 152098960 synonymous variant G/A snv 0.19 0.18 16
rs3798577
ESR1
0.742 0.320 6 152099995 3 prime UTR variant T/C snv 0.45 16
rs201820837
ETV6
0.925 0.040 12 11869532 missense variant G/A;T snv 2.4E-05; 6.4E-05 2
rs4246215
FADS2 ; FEN1
0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 29