Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10459012 11 55324098 upstream gene variant C/A snv 0.25 1
rs2789047 6 120868656 intergenic variant C/A;G;T snv 1
rs62412107 4 9540731 regulatory region variant G/A;T snv 1
rs819196 8 23885208 intergenic variant T/A snv 0.61 1
rs898696 7 155879955 intergenic variant T/G snv 0.58 1
rs9887774 1 23375891 downstream gene variant A/C snv 1
rs10262995
BBS9
7 33510429 intron variant C/T snv 9.1E-02 1
rs10062079
C9 ; DAB2
5 39393631 intron variant G/A snv 0.39 1
rs16972495
CEMIP
15 80856398 intron variant A/C snv 0.15 1
rs75530000
CHAF1B
21 36408748 intron variant C/T snv 8.1E-02 4.5E-02 1
rs2762943
CYP24A1
20 54174247 upstream gene variant T/G snv 0.94 1
rs8072297
FBXL20
17 39321795 intron variant A/C;G;T snv 1
rs115151282
HLA-DQA1
6 32632634 intron variant C/T snv 1
rs10794486
IGF1R
15 98758306 intron variant G/A;T snv 1
rs548873184
LINC00626
1 168785175 intron variant G/A;T snv 1.3E-04 1
rs13317787
LMCD1-AS1
3 8100265 intron variant C/A snv 6.7E-02 1
rs35925637
LOC101928278
2 216811905 intron variant T/A snv 0.46 1
rs111653425
LOC105371578 ; SLC47A1
17 19571562 missense variant C/T snv 6.4E-03 6.1E-03 1
rs17257827
LOC105379011
5 68519186 intron variant A/G snv 0.14 1
rs142093111
LRP2
2 169188258 missense variant G/A snv 1.7E-04 2.2E-04 1
rs17001974
MRTFA
22 40481380 intron variant C/T snv 0.12 1
rs6060139
MYH7B
20 34978696 intron variant T/C snv 0.62 1
rs4237268
PIP5K1B
9 68843260 non coding transcript exon variant G/A snv 0.70 1
rs143933372
PSORS1C1
6 31131462 intron variant T/C snv 2.5E-03 1
rs34400381
SLC25A45
11 65376421 missense variant G/A snv 2.6E-02 2.4E-02 1