Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1447826 1.000 0.120 3 74669607 intergenic variant T/A;C;G snv 1
rs2172905 1.000 0.120 6 170019278 regulatory region variant C/T snv 0.30 1
rs2903018 1.000 0.120 19 29164379 intergenic variant G/A;T snv 1
rs1153287
BACH1
1.000 0.120 21 29313290 intron variant G/A;T snv 1
rs1153294
BACH1
1.000 0.120 21 29328775 intron variant T/C;G snv 1
rs117214
BACH1
1.000 0.120 21 29348513 intron variant C/T snv 0.45 1
rs2832290
BACH1
1.000 0.120 21 29356542 intron variant A/G snv 0.48 1
rs7015626
LINC00964
1.000 0.120 8 124864572 intron variant G/A snv 0.39 1
rs2035565
LINC01829
1.000 0.120 2 67392524 intron variant C/T snv 0.74 1
rs1555461176
PALB2
1.000 0.120 16 23634893 stop gained -/T delins 1
rs1975920
PPFIBP1
1.000 0.120 12 27583053 intron variant G/T snv 0.40 1
rs7106914
SBF2
1.000 0.120 11 9956424 intron variant T/C snv 0.38 1
rs10887710 0.925 0.120 10 80270029 downstream gene variant T/C snv 0.19 2
rs1552462 0.925 0.120 11 7235910 upstream gene variant C/T snv 2.7E-02 2
rs6001516 0.925 0.120 22 39248198 intron variant C/T snv 6.1E-02 2
rs9573163 0.925 0.120 13 73334709 regulatory region variant C/G;T snv 2
rs1153280
BACH1
1.000 0.120 21 29305751 intron variant G/A snv 0.52 2
rs708224
BICD1
0.925 0.120 12 32283475 intron variant A/G snv 0.50 2
rs80358451
BRCA2
0.925 0.160 13 32333140 missense variant T/G snv 5.6E-05 6.3E-05 2
rs11644043
BRD7
0.925 0.120 16 50327466 intron variant T/C snv 0.24 2
rs782128510
C17orf97 ; LOC105371430
0.925 0.120 17 410373 missense variant C/A;G snv 7.6E-05; 8.4E-06 2
rs2255280
C9 ; DAB2
0.925 0.120 5 39394887 intron variant C/A snv 0.98 2
rs1276300653
CAMK1 ; OGG1
0.925 0.120 3 9757072 missense variant T/C snv 7.0E-06 2
rs1800843
CCKBR
0.925 0.120 11 6270835 synonymous variant C/A;G snv 0.16; 4.0E-06 0.19 2
rs1336539869
CDK4
0.925 0.120 12 57751681 missense variant C/G snv 2