Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3783347
WARS1
14 100372924 intron variant G/T snv 0.16 2
rs12385797 11 106465562 upstream gene variant C/A snv 6.4E-02 1
rs16913693
ELP1
9 108918079 intron variant T/G snv 8.4E-02 2
rs118137427 10 111217250 intergenic variant A/G snv 3.3E-02 2
rs11195502 10 111279909 intergenic variant C/A;G;T snv 2
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 4
rs17747324
TCF7L2
0.925 0.160 10 112992744 intron variant T/C snv 0.17 4
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12243326
TCF7L2
0.925 0.160 10 113029056 intron variant T/C snv 0.27 5
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs4682484
CFAP44
3 113304023 missense variant T/A;C snv 0.98 1
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 5
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs35859536
LOC105375716
8 117179236 downstream gene variant C/T snv 0.25 2
rs17667932
MED30
1.000 0.120 8 117537137 intron variant T/C snv 7.5E-02 2
rs10849893
KDM2B
12 121500382 intron variant C/G snv 0.30 1
rs12285364
SORL1
1.000 0.080 11 121522517 intron variant C/T snv 6.7E-02 2
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 4
rs4836906 9 122665528 downstream gene variant T/C snv 1.6E-02 1
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 9
rs11717195
ADCY5
1.000 0.080 3 123363551 intron variant T/C snv 0.19 3
rs2877716
ADCY5
3 123375604 intron variant T/C snv 0.76 4
rs117911989
MKLN1
7 131285034 intron variant G/A;C snv 2