Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12294104
LOC102723403
11 30361352 intergenic variant C/T snv 0.14 4
rs148982377
ZNF789 ; ZNF394
7 99477415 intron variant T/C snv 3.2E-02 4
rs17277546
TRIM4
7 99891948 3 prime UTR variant G/A snv 3.1E-02 4
rs7860634
LHX3
9 136197833 intron variant G/A snv 0.55 4
rs10032216
LOC107986195
4 148748354 intron variant T/A;C snv 3
rs10799824
LOC105376819 ; LOC105376817 ; MICOS10
1 19514680 intron variant G/A snv 0.18 3
rs11624776 14 93129246 regulatory region variant A/C;T snv 3
rs11726248 4 170132368 intergenic variant G/A snv 6.8E-02 3
rs117585797
LOC105369621 ; ANO2
12 5902324 intron variant C/A snv 1.1E-02 3
rs3813582
LINC01229 ; LOC105371356 ; MAFTRR
16 79715456 non coding transcript exon variant T/C snv 0.28 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
rs7240777 18 73500517 intergenic variant G/A snv 0.53 3
rs10215854
PTCD1 ; CPSF4 ; ATP5MF-PTCD1
7 99439297 intron variant G/A snv 0.19 2
rs10278040 7 99543750 downstream gene variant G/A snv 0.16 2
rs10519227
FAM227B ; FGF7
15 49454167 intron variant T/A snv 0.20 2
rs10744816 12 114276461 regulatory region variant T/C snv 0.39 2
rs11031002
LOC105376607
11 30193714 intron variant T/A snv 0.10 2
rs112295236
SLC22A10
11 63147874 intron variant C/A;G snv 2
rs117145500 16 52913718 intergenic variant A/C snv 4.8E-02 2
rs11755845
LINC01512
6 43937043 regulatory region variant C/T snv 0.21 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