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
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs1491850 0.925 0.080 11 27728178 intron variant T/C snv 0.37 6
rs6547692
GCKR
1.000 0.080 2 27512105 intron variant G/A snv 0.58 3
rs35397826
ARSG ; SLC16A6
17 68273941 missense variant A/G snv 0.12 0.11 2
rs113918189
CEP83
12 94325241 intron variant C/T snv 6.9E-02 2
rs2984348
CITED1 ; LOC105373250
X 72308510 intron variant C/T snv 0.31 2
rs7113624
LOC107984361
11 87508051 regulatory region variant G/A;C snv 2
rs7215775
TBX2
17 61406955 non coding transcript exon variant A/G snv 0.68 2
rs7495833
WDR72
15 53651121 intron variant C/A snv 0.37 2
rs11109815 12 78449114 non coding transcript exon variant G/A snv 9.1E-03 1
rs12910301 15 50770120 upstream gene variant A/G snv 0.12 1
rs459044
BCAS1
20 54062115 intron variant A/G snv 0.64 1
rs9350272
CDKAL1
6 20720587 intron variant A/C;G;T snv 1
rs4848713
CLASP1
2 121605302 intron variant C/T snv 0.12 1
rs116817194
HLA-DRA
6 32443746 intron variant T/A;C snv 1
rs62049973
NFAT5
16 69666298 intron variant A/G snv 0.10 1
rs3948714
RPH3A
12 112862964 intron variant T/C snv 0.49 1
rs73351820
WBP1L
10 102810527 intron variant T/A;C;G snv 1