Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs1495743 8 18415790 intergenic variant G/A;C snv 6
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs17277546
TRIM4
7 99891948 3 prime UTR variant G/A snv 3.1E-02 4
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 4
rs477992
PHGDH
1 119714953 intron variant A/G snv 0.69 4
rs60808706
KCNQ1
11 2836003 intron variant G/A snv 0.12 4
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 4
rs8396
ETFDH ; PPID
4 158709665 3 prime UTR variant T/C snv 0.29 4
rs11185790
PANK1
10 89612776 intron variant G/A snv 0.15 3
rs11924032
SLC2A2
3 171017310 intron variant G/A snv 0.29 3
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 3
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv 3
rs211718
SLC44A5
1 75640990 downstream gene variant T/C snv 0.75 3
rs2232326
SPC25 ; G6PC2
2 168907981 missense variant T/C snv 5.1E-03 3.3E-03 3
rs2624265
LINC02694
15 38856448 intron variant T/C snv 0.28 3
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 3
rs61824877
LINC00862
1 200273504 intron variant G/A snv 0.11 3
rs7760535
REV3L ; MFSD4B
6 111425880 intron variant G/C snv 0.46 3
rs9393903
ELOVL2 ; ELOVL2-AS1
6 11042676 intron variant G/A snv 0.18 3
rs9943291
HMGCS2
1 119749667 intron variant T/G snv 8.2E-02 3
rs10518693
IVD
15 40407823 intron variant C/T snv 0.37 2
rs10799701 1 21494497 intergenic variant A/G snv 0.47 2