Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs4409766
BORCS7-ASMT ; BORCS7
1.000 0.040 10 102856906 intron variant T/C snv 0.14 1
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 4
rs2967951
LOC105369214 ; ROPN1L
5 10463995 intron variant C/T snv 0.19 2
rs3934834
LOC105378948 ; LOC112267874
1 1070426 downstream gene variant C/T snv 0.21 2
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs518785 1 110817180 regulatory region variant G/A snv 0.82 1
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 10
rs10885122 1.000 0.080 10 111282335 intergenic variant T/G snv 0.71 3
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 10
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 3
rs4833407
ALPK1
1.000 0.080 4 112390634 intron variant C/A;T snv 1
rs2891403
RPH3A
1.000 0.040 12 112699767 intron variant A/G;T snv 1
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs12243326
TCF7L2
0.925 0.160 10 113029056 intron variant T/C snv 0.27 1
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs3802177
SLC30A8 ; LOC105375716
1.000 0.080 8 117172786 3 prime UTR variant G/A snv 0.24 3
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs7534091 1 118321993 intergenic variant A/G snv 0.23 1
rs984222
TBX15
1 118961220 intron variant C/A;G snv 1
rs308971
SYN2
3 12075120 intron variant G/A snv 0.82 2
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 3