Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs57884925
GLIS3
9 4285119 intron variant C/G;T snv 2
rs2232326
SPC25 ; G6PC2
2 168907981 missense variant T/C snv 5.1E-03 3.3E-03 3
rs3765467
GLP1R
1.000 0.080 6 39065819 missense variant G/A;C;T snv 3.6E-02 1.2E-02 3
rs76185967
RPL35P6 ; PSD3
8 18774816 non coding transcript exon variant C/T snv 1.6E-02 2
rs17277546
TRIM4
7 99891948 3 prime UTR variant G/A snv 3.1E-02 4
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs12053049
SPC25
2 168910638 intron variant T/C snv 5.2E-02 2
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs12369179
ZCCHC8
0.851 0.120 12 122479003 intron variant C/T snv 5.9E-02 16
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs2023634
DGCR9 ; DGCR5
22 18984937 intron variant A/G snv 7.9E-02 2
rs9943291
HMGCS2
1 119749667 intron variant T/G snv 8.2E-02 3
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs61824877
LINC00862
1 200273504 intron variant G/A snv 0.11 3
rs60808706
KCNQ1
11 2836003 intron variant G/A snv 0.12 4
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs7094971
SLC16A9
0.925 0.120 10 59689806 intron variant A/G snv 0.13 4
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs662138
SLC22A1
6 160143444 intron variant C/G snv 0.14 2
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 4
rs6558295
GPAA1
8 144084619 intron variant C/G snv 8.1E-02 0.14 2