Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6558295
GPAA1
8 144084619 intron variant C/G snv 8.1E-02 0.14 2
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 5
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs1558318 1.000 0.080 7 15025987 intergenic variant A/T snv 0.55 3
rs7200543
PDXDC1
16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs8396
ETFDH ; PPID
4 158709665 3 prime UTR variant T/C snv 0.29 4
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
rs662138
SLC22A1
6 160143444 intron variant C/G snv 0.14 2
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 18
rs2232326
SPC25 ; G6PC2
2 168907981 missense variant T/C snv 5.1E-03 3.3E-03 3
rs12053049
SPC25
2 168910638 intron variant T/C snv 5.2E-02 2
rs11924032
SLC2A2
3 171017310 intron variant G/A snv 0.29 3
rs12670403
LOC101927609 ; AHR
7 17269655 intron variant C/A snv 0.46 2
rs1349497
RAPGEF4-AS1
2 172727935 intron variant G/A;C snv 2
rs2403254
HPS5
11 18303599 intron variant C/G;T snv 2
rs1495743 8 18415790 intergenic variant G/A;C snv 6
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 3
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 3
rs76185967
RPL35P6 ; PSD3
8 18774816 non coding transcript exon variant C/T snv 1.6E-02 2
rs2023634
DGCR9 ; DGCR5
22 18984937 intron variant A/G snv 7.9E-02 2
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 8
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18