Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs2853961 6 31264212 downstream gene variant G/A snv 0.38 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs76792961
FAM234A
16 243594 intron variant C/T snv 7.3E-03 13
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs3811444
TRIM58
1 247876149 missense variant C/T snv 0.31 0.26 12
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs17342717
SLC17A1
6 25821542 intron variant C/T snv 6.1E-02 8
rs2075672
TFR2 ; ACTL6B
7 100642673 intron variant A/G snv 0.65 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 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
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 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