Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2509851
DPAGT1 ; H2AX
11 119096070 upstream gene variant A/C snv 0.30 1
rs2921060
LOC107986913
8 8460307 intron variant A/C snv 0.55 1
rs34647824
RRAS
19 49634886 downstream gene variant A/C snv 0.34 1
rs35154268
SND1
7 127865702 intron variant A/C snv 0.22 1
rs35732522
SLC8A1
2 40486025 intron variant A/C snv 0.31 1
rs4525087
ZNF436
1 23365736 intron variant A/C snv 0.58 1
rs56255430 19 19367068 TF binding site variant A/C snv 6.0E-02 1
rs61830291
LINC01352
1 220827800 intron variant A/C snv 6.3E-02 1
rs61993680
SLC25A29
14 100286307 intron variant A/C snv 0.39 1
rs6780429 3 30708912 regulatory region variant A/C snv 0.48 1
rs690428
WDR72
15 53658381 intron variant A/C snv 0.35 1
rs7203398
CHD9
16 53155760 intron variant A/C snv 0.26 1
rs72834794
MED24
17 40055130 intron variant A/C snv 6.0E-02 1
rs755631
LRP2
2 169150430 intron variant A/C snv 0.49 1
rs76112240
MECOM
3 169418126 intron variant A/C snv 0.12 1
rs7719168
ARL15
5 53996560 intron variant A/C snv 8.7E-02 1
rs81205
KCNQ1
11 2777574 intron variant A/C snv 0.56 1
rs497309
CYP21A2 ; C2
0.882 0.240 6 31924707 intron variant A/C;G snv 5
rs2542713
DAB2 ; C9
1.000 0.040 5 39385539 intron variant A/C;G snv 3
rs1705694 8 23912105 intergenic variant A/C;G snv 0.50 2
rs17169194
UMAD1 ; RPA3
7 7641066 5 prime UTR variant A/C;G snv 2
rs56376587
NFATC1 ; LOC107985163
18 79400235 intron variant A/C;G snv 2
rs7187776
TUFM ; SH2B1
16 28846324 5 prime UTR variant A/C;G snv 2
rs3822939
EYA4 ; TARID
6 133528651 intron variant A/C;G snv 1
rs7187910 16 89671938 non coding transcript exon variant A/C;G snv 1