Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3753584
MTHFR ; CLCN6
0.827 0.080 1 11804529 5 prime UTR variant T/C snv 0.14 10
rs17367504
MTHFR
1.000 0.040 1 11802721 intron variant A/G snv 0.14 9
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs2932538
MOV10
1 112673921 intron variant A/C;G snv 4
rs17037452
CLCN6
1 11835618 intron variant A/G snv 0.18 3
rs1731249
KCNK3
2 26697157 intron variant T/A snv 0.48 5
rs438885 2 164195781 intron variant A/T snv 0.56 5
rs7577262 2 233910224 intergenic variant G/A;T snv 4
rs11693319
CCDC141
2 178873542 3 prime UTR variant C/G;T snv 2
rs1290784
MECOM
3 169379112 intron variant C/A;T snv 6
rs419076
MECOM
3 169383098 intron variant T/A;C snv 6
rs448378
MECOM
1.000 0.040 3 169383111 intron variant G/A;C snv 5
rs3774372
ULK4
1.000 0.160 3 41835922 missense variant T/C snv 0.17 0.18 4
rs2014590
MECOM
3 169428709 intron variant C/T snv 0.53 2
rs60605842
SLC4A7
3 27439550 intron variant A/G snv 0.29 2
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs13139571
LOC107984032 ; GUCY1A1
1.000 0.040 4 155724361 intron variant C/A snv 0.22 9
rs11099097 4 80246155 intergenic variant C/T snv 0.30 6
rs1596724
LOC107986223
4 32554231 intergenic variant T/C snv 5.9E-02 2
rs4460079
ARSJ
4 113940144 intron variant C/T snv 0.58 2
rs7658266
ARSJ
4 113942550 intron variant T/A;C snv 2
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs11953630 5 158418394 intergenic variant C/A;T snv 6