Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10273424
TMEM225B
0.925 0.080 7 99598450 intron variant T/A snv 0.13 3
rs10278040 7 99543750 downstream gene variant G/A snv 0.16 2
rs10744816 12 114276461 regulatory region variant T/C snv 0.39 2
rs117145500 16 52913718 intergenic variant A/C snv 4.8E-02 2
rs1624802 12 130012927 intergenic variant A/G;T snv 2
rs17776563 15 88575873 intergenic variant G/A;C snv 2
rs2497304 1.000 0.080 10 92732959 intergenic variant C/T snv 0.36 2
rs2910397 1.000 0.120 19 47894860 intergenic variant C/T snv 0.38 2
rs740160
ARPC1A
1.000 0.120 7 99360257 intron variant C/T snv 8.6E-02 2
rs7608623
ATAD2B
2 23726083 intergenic variant G/T snv 0.57 2
rs17250196
CASTOR3 ; PVRIG ; STAG3
7 100219573 3 prime UTR variant G/A;T snv 2
rs10519227
FAM227B ; FGF7
15 49454167 intron variant T/A snv 0.20 2
rs12659622
FBXL7
5 15618072 intron variant G/A snv 8.3E-02 2
rs1571583
GLIS3
9 4267209 intron variant A/G snv 0.77 2
rs11755845
LINC01512
6 43937043 regulatory region variant C/T snv 0.21 2
rs182420
LINC01595
1.000 0.040 19 47868938 upstream gene variant C/T snv 0.80 2
rs13015993
LOC101928278
2 216760800 intron variant G/A snv 0.64 2
rs11031002
LOC105376607
11 30193714 intron variant T/A snv 0.10 2
rs58926603
LOC107985017
17 6438550 upstream gene variant A/G snv 0.47 2
rs58632700
LOC112268251 ; SLC27A5 ; ZNF446
19 58480634 missense variant C/T snv 1.0E-03 2.8E-04 2
rs758970
MVB12B
9 126432494 intron variant A/G snv 0.58 2
rs334699
NFIA
1 61154824 intron variant A/G snv 0.92 2
rs7825175
NRG1
8 32558756 intron variant G/A snv 0.18 2
rs753760
PDE10A
6 165632995 intron variant C/A;G snv 2
rs3981351
PLEKHS1
10 113755361 5 prime UTR variant G/A;T snv 2