Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs2235544
DIO1
0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 14
rs34670419
ZKSCAN5
1.000 0.080 7 99533211 3 prime UTR variant G/A;T snv 7.7E-06; 2.6E-02 7
rs9472138
LOC107986598
0.882 0.160 6 43844025 downstream gene variant C/T snv 0.24 6
rs11031005
LOC105376607
1.000 0.120 11 30204809 intron variant T/C snv 0.10 5
rs4646450
CYP3A5 ; ZSCAN25
0.882 0.120 7 99668695 3 prime UTR variant G/A snv 0.38 4
rs7860634
LHX3
9 136197833 intron variant G/A snv 0.55 4
rs12294104
LOC102723403
11 30361352 intergenic variant C/T snv 0.14 4
rs6885099
PDE8B
1.000 0.040 5 77234524 intron variant A/G snv 0.52 4
rs17277546
TRIM4
7 99891948 3 prime UTR variant G/A snv 3.1E-02 4
rs11761528
ZKSCAN5
1.000 0.120 7 99521178 intron variant C/T snv 0.12 4
rs10235235
ZNF394 ; ZNF789
0.925 0.080 7 99478208 intron variant T/C snv 0.13 4
rs148982377
ZNF789 ; ZNF394
7 99477415 intron variant T/C snv 3.2E-02 4
rs11624776 14 93129246 regulatory region variant A/C;T snv 3
rs11726248 4 170132368 intergenic variant G/A snv 6.8E-02 3
rs7240777 18 73500517 intergenic variant G/A snv 0.53 3
rs4804416
INSR
19 7223837 intron variant T/G snv 0.37 3
rs1537424
LINC00609
1.000 0.040 14 36104812 intron variant C/T snv 0.49 3
rs3813582
LINC01229 ; LOC105371356 ; MAFTRR
16 79715456 non coding transcript exon variant T/C snv 0.28 3
rs117585797
LOC105369621 ; ANO2
12 5902324 intron variant C/A snv 1.1E-02 3
rs10799824
LOC105376819 ; LOC105376817 ; MICOS10
1 19514680 intron variant G/A snv 0.18 3
rs10032216
LOC107986195
4 148748354 intron variant T/A;C snv 3
rs6499766
LPCAT2
16 55570216 intron variant A/T snv 0.54 3
rs7045138
PTCSC2
9 97829181 intron variant C/G;T snv 3
rs9497965
SASH1
1.000 0.040 6 148200156 regulatory region variant C/T snv 0.40 3