Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs439680 1.000 0.080 5 109998341 regulatory region variant C/G snv 3
rs114033761 1.000 0.080 6 31093784 regulatory region variant T/C snv 1
rs141670911 1.000 0.080 6 26581030 intergenic variant A/T snv 7.3E-02 1
rs141877527 1.000 0.080 10 33497992 intergenic variant A/G snv 7.3E-03 1
rs312599 1.000 0.080 5 143998425 intergenic variant C/T snv 0.33 1
rs716274 1.000 0.080 11 103547430 intergenic variant A/G snv 0.51 1
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs717620
ABCC2
0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs17185553
ADAMTSL1
1.000 0.080 9 17934122 intron variant G/C snv 6.5E-02 1
rs74501188
ADGRV1
1.000 0.080 5 90931162 5 prime UTR variant G/A snv 0.17 1
rs4513061
AGBL1
0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519877
B2M ; PATL2
0.763 0.280 15 44711549 start lost G/A snv 10
rs2279115
BCL2
0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv 18
rs140013431
BMP6
1.000 0.080 6 7770278 intron variant T/C snv 1.2E-02 1
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs12200782
BTN3A1
1.000 0.080 6 26402808 intron variant C/G snv 7.9E-02 1
rs4353229
CASP7
0.807 0.160 10 113729830 3 prime UTR variant T/C snv 0.23 6
rs1045494
CASP8
0.882 0.120 2 201287058 3 prime UTR variant T/C snv 0.10 3
rs1535045
CD40
0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs55853698
CHRNA5
0.882 0.080 15 78565597 5 prime UTR variant T/G snv 0.25 5