Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10032216
LOC107986195
4 148748354 intron variant T/A;C snv 3
rs1011024
TMEM225B
7 99599778 intron variant A/G snv 0.38 1
rs1017993 19 47900919 intergenic variant C/T snv 0.11 1
rs10215854
PTCD1 ; CPSF4 ; ATP5MF-PTCD1
7 99439297 intron variant G/A snv 0.19 2
rs10226310
ZKSCAN5
7 99520697 intron variant G/A snv 0.13 1
rs10235235
ZNF394 ; ZNF789
0.925 0.080 7 99478208 intron variant T/C snv 0.13 4
rs10238965
FAM200A
7 99548222 missense variant C/A;T snv 0.26 1
rs10254729
TMEM225B
7 99598805 intron variant T/G snv 0.38 1
rs10271049
PTCD1 ; ATP5MF-PTCD1
7 99428870 intron variant A/G snv 0.38 1
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
rs10410350 19 47849107 regulatory region variant A/G snv 0.18 1
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
rs10799824
LOC105376819 ; LOC105376817 ; MICOS10
1 19514680 intron variant G/A snv 0.18 3
rs10808111
ZNF789
7 99473261 intron variant T/A snv 0.12 1
rs10808112
ZNF789
7 99473365 intron variant C/T snv 0.19 1
rs11031002
LOC105376607
11 30193714 intron variant T/A snv 0.10 2
rs11031005
LOC105376607
1.000 0.120 11 30204809 intron variant T/C snv 0.10 5
rs112295236
SLC22A10
11 63147874 intron variant C/A;G snv 2
rs11572169
CYP2C8
10 95040017 intron variant T/C snv 8.0E-02 1
rs11624776 14 93129246 regulatory region variant A/C;T snv 3
rs117145500 16 52913718 intergenic variant A/C snv 4.8E-02 2
rs11726248 4 170132368 intergenic variant G/A snv 6.8E-02 3
rs11755845
LINC01512
6 43937043 regulatory region variant C/T snv 0.21 2