Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35979828
NFE2
12 54292096 intron variant C/T snv 5.0E-02 9
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs17342717
SLC17A1
6 25821542 intron variant C/T snv 6.1E-02 8
rs17476364
HK1
10 69334748 intron variant T/C snv 6.4E-02 8
rs9487023
CCDC162P
6 109268801 intron variant A/G snv 0.40 8
rs10758656
RCL1
9 4852599 intron variant A/G snv 0.19 7
rs129128
H2BC4 ; H2AC6
6 26125114 intron variant C/T snv 0.91 7
rs1505307
THRB
3 24301839 intron variant T/C snv 0.60 7
rs17534202 1.000 0.120 1 203312047 downstream gene variant G/C snv 0.40 7
rs2283847
MN1
22 27785411 intron variant C/A;G;T snv 7
rs7203560
NPRL3
1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 7
rs7225002
KANSL1
0.925 0.080 17 46111701 intron variant A/G snv 0.39 7
rs737092 20 57415349 regulatory region variant T/C snv 0.58 7
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
rs12216125 0.925 0.120 6 25997230 intron variant C/T snv 0.26 6
rs130624 22 37042611 regulatory region variant G/T snv 0.47 6
rs1434282
LINC01221
1 199041592 non coding transcript exon variant C/T snv 0.76 6
rs144861591 6 26072764 intergenic variant C/T snv 3.8E-02 6
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs218237 4 54528005 intergenic variant C/T snv 0.18 6
rs228129
LOC112268295
22 37032558 upstream gene variant A/G snv 0.48 6
rs2413450
TMPRSS6
22 37074184 intron variant T/C snv 0.61 6
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs35158985
CDH1
0.882 0.080 16 68762843 intron variant A/G snv 0.38 6
rs3887266
SLC17A3
0.925 0.120 6 25843518 intron variant C/T snv 8.9E-02 6