Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
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
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs601338
FUT2 ; LOC105447645
0.742 0.280 19 48703417 stop gained G/A snv 0.38 0.45 19
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 18
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 9
rs2393791
HNF1A
0.925 0.160 12 120986153 intron variant C/T snv 0.62 8
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 7
rs12539316 0.925 0.120 7 73563568 downstream gene variant A/G snv 0.28 6
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 6
rs4820599
LRRC75B ; GGT1
0.925 0.160 22 24594246 intron variant A/G snv 0.43 6
rs4835265
ZNF827
4 145900258 intron variant C/A snv 0.15 6
rs11066453
OAS1
1.000 0.080 12 112927816 intron variant A/G snv 3.8E-03 4
rs13395911
EFHD1
2 232655544 intron variant A/T snv 0.59 3
rs944002
EXOC3L4
14 103106478 intron variant A/G snv 0.25 3
rs3213545
OASL
12 121033534 synonymous variant G/A snv 0.32 0.26 3
rs235314
PTTG1IP
21 44851537 missense variant C/T snv 0.48 0.46 3
rs340005
RORA-AS1 ; RORA
15 60585831 intron variant G/A snv 0.67 3
rs17157266 1.000 0.040 11 62432345 downstream gene variant T/C snv 0.14 2
rs7786376 7 73628284 upstream gene variant A/G snv 0.28 2
rs12968116
ATP8B1 ; LOC100505549
18 57655270 missense variant C/T snv 8.2E-02 8.0E-02 2