Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 14
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 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
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 13
rs9917425
OTOR
20 16755400 intron variant G/T snv 0.16 13
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs10224210
PRKAG2
1.000 0.040 7 151716108 intron variant T/C snv 0.21 9