Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 13
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 11
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 11
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 10
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 10
rs9376092
LOC105378010
0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 10
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs17342717
SLC17A1
6 25821542 intron variant C/T snv 6.1E-02 8
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 7
rs737092 20 57415349 regulatory region variant T/C snv 0.58 7
rs8176743
ABO
1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11 7
rs13006529
CASP10
0.851 0.080 2 201217736 missense variant T/A snv 0.41 0.42 7
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7