Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4769793 0.807 0.120 13 29985289 intergenic variant G/C snv 8
rs2069852 0.925 0.080 7 22732641 downstream gene variant G/A;C snv 4
rs7240004 1.000 0.040 18 48868651 intergenic variant A/G snv 0.43 4
rs1194338 0.925 0.080 11 65493967 upstream gene variant C/A;T snv 3
rs2660852 12 96051770 intergenic variant C/A snv 0.34 3
rs1056123575
ADAMTS1
0.925 0.080 21 26844557 missense variant G/A snv 4.2E-06 7.0E-06 4
rs772893086
ADARB1
0.925 0.080 21 45176099 missense variant A/C;G;T snv 4.0E-06 4
rs4024
AFP
0.827 0.120 4 73435667 intron variant G/A snv 0.52 7
rs737241
AFP
0.827 0.120 4 73451012 intron variant G/A;C snv 7
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs1200003171
AKT1
0.882 0.120 14 104775122 missense variant C/A;T snv 8.0E-06 4
rs1383618437
ATAT1
6 30627473 missense variant C/A snv 4.0E-06 1
rs774390402
BCAR1
16 75235116 missense variant A/C snv 1.2E-05 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs80358829
BRCA2
0.827 0.120 13 32340327 missense variant C/T snv 6
rs3917412
C1orf112 ; SELE
1.000 0.040 1 169731361 intron variant T/A;C;G snv 4
rs3829078
CA9
0.851 0.160 9 35679254 missense variant A/G;T snv 8.2E-02 6
rs750802459
CASP3
1.000 0.120 4 184635342 frameshift variant TCAGGATAATCCATTTTATAACTGTTGTCCAGGGATATTCCAGAGTC/- delins 5.6E-05 2
rs1213469537
CAV1
0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 9
rs1172398253
CCN1
0.925 0.080 1 85582045 missense variant C/T snv 4.0E-06 4
rs735482
CD3EAP ; ERCC1
0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs1451539938
CD82
0.925 0.080 11 44618361 missense variant A/G snv 4.1E-06 7.0E-06 3