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
rs11031005
LOC105376607
1.000 0.120 11 30204809 intron variant T/C snv 0.10 5
rs10235235
ZNF394 ; ZNF789
0.925 0.080 7 99478208 intron variant T/C snv 0.13 4
rs11761528
ZKSCAN5
1.000 0.120 7 99521178 intron variant C/T snv 0.12 4
rs148982377
ZNF789 ; ZNF394
7 99477415 intron variant T/C snv 3.2E-02 4
rs6885099
PDE8B
1.000 0.040 5 77234524 intron variant A/G snv 0.52 4
rs7860634
LHX3
9 136197833 intron variant G/A snv 0.55 4
rs10032216
LOC107986195
4 148748354 intron variant T/A;C snv 3
rs10273424
TMEM225B
0.925 0.080 7 99598450 intron variant T/A snv 0.13 3
rs10799824
LOC105376819 ; LOC105376817 ; MICOS10
1 19514680 intron variant G/A snv 0.18 3
rs117585797
LOC105369621 ; ANO2
12 5902324 intron variant C/A snv 1.1E-02 3
rs1537424
LINC00609
1.000 0.040 14 36104812 intron variant C/T snv 0.49 3
rs4804416
INSR
19 7223837 intron variant T/G snv 0.37 3
rs6499766
LPCAT2
16 55570216 intron variant A/T snv 0.54 3
rs7045138
PTCSC2
9 97829181 intron variant C/G;T snv 3
rs10215854
PTCD1 ; CPSF4 ; ATP5MF-PTCD1
7 99439297 intron variant G/A snv 0.19 2
rs10519227
FAM227B ; FGF7
15 49454167 intron variant T/A snv 0.20 2
rs11031002
LOC105376607
11 30193714 intron variant T/A snv 0.10 2
rs112295236
SLC22A10
11 63147874 intron variant C/A;G snv 2
rs12659622
FBXL7
5 15618072 intron variant G/A snv 8.3E-02 2
rs13015993
LOC101928278
2 216760800 intron variant G/A snv 0.64 2
rs13222543
ZCWPW1
7 100417834 intron variant C/T snv 1.2E-02 2
rs1571583
GLIS3
9 4267209 intron variant A/G snv 0.77 2
rs17723470
PRDM11
11 45206016 intron variant C/T snv 0.21 2