Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 13
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs3123543
ATF3
1 212617344 intron variant T/A;C snv 13
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 13
rs3840870
COL1A1
17 50184820 3 prime UTR variant -/CTTG delins 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
rs7296503
PDZRN4
12 41306962 intron variant C/T snv 0.57 13
rs4837892
TTLL11
9 121826025 intron variant G/T snv 0.36 13
rs8176746
ABO
0.882 0.160 9 133255935 missense variant G/A;T snv 4.1E-06; 0.12 12
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 12
rs10224002
PRKAG2
0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 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
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs649129 1.000 0.080 9 133278860 upstream gene variant T/C;G snv 10
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
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