Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs114165349
LOC101928728 ; ARID1A
1 26695422 intron variant G/C snv 1.7E-02 5
rs11636952
LMAN1L
15 74821981 intron variant T/C snv 0.48 5
rs11725969
GUCY1A1
4 155705436 intron variant C/T snv 0.24 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs13209747 6 126794309 intron variant C/G;T snv 0.36 5
rs1573643
FURIN
15 90877743 intron variant T/C snv 0.33 5
rs1799852
TF
3 133756878 synonymous variant C/T snv 0.13 0.11 5
rs1813353
CACNB2
10 18418519 intron variant T/C snv 0.29 5
rs1894400
FES
15 90885725 intron variant C/T snv 0.28 5
rs2004776
AGT
1 230712956 intron variant C/G;T snv 5
rs2013002 12 111762346 intron variant T/A;C snv 5
rs2043082
ALDH1A2
15 58382109 intron variant G/A snv 0.32 5
rs2304128
GMIP
19 19635342 intron variant G/C;T snv 5
rs2763981
CYP21A2 ; SLC44A4
6 31872244 intron variant T/A snv 0.79 5
rs35441 12 115115310 intergenic variant C/T snv 0.40 5
rs35443 12 115115073 intergenic variant G/C snv 0.40 5
rs4495740
DOCK7
1 62658794 intron variant T/G snv 0.34 5
rs4722551
LOC105375199
7 25952206 upstream gene variant T/C;G snv 5
rs4980389
LSP1
11 1871355 5 prime UTR variant G/A snv 0.35 5
rs509728 11 116662450 downstream gene variant G/C snv 2.7E-02 5
rs6108787 20 10986566 intron variant T/G snv 0.46 5
rs62033406
FTO
16 53790314 intron variant A/G snv 0.33 5
rs7096937
GPAM
10 112190660 intron variant T/C snv 0.72 5
rs7125196
LOC105369329
11 61505093 intron variant T/C snv 0.16 5
rs7953257
HECTD4
12 112246417 intron variant A/G;T snv 0.71 5