Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02 5
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs806321
DLEU1
0.851 0.160 13 50267187 intron variant C/T snv 0.47 4
rs1239948
DLEU1 ; DLEU7
13 50532386 intron variant A/T snv 0.59 3
rs963740
DLEU7 ; DLEU1 ; DLEU1-AS1
1.000 0.080 13 50521959 intron variant A/T snv 0.28 2
rs41284816
DLEU1 ; DLEU2
13 50081853 non coding transcript exon variant G/C;T snv 2
rs1149833
DLEU1
0.925 0.160 13 50176740 intron variant A/T snv 0.47 2
rs806293
DLEU1
13 50238846 intron variant T/A snv 0.47 2
rs797486
DLEU7 ; DLEU1
13 50647482 intron variant C/A snv 0.85 2
rs797487
DLEU1 ; DLEU7
0.925 0.040 13 50650173 intron variant T/G snv 0.56 2
rs6561599
DLEU1 ; RNASEH2B-AS1
1.000 0.040 13 50904782 non coding transcript exon variant C/G snv 0.61 2
rs1638703
DLEU1
1.000 0.040 13 50514220 intron variant G/C snv 0.27 2
rs1239704
DLEU7 ; DLEU1
13 50578475 intron variant G/A;T snv 1
rs1568672
DLEU1
13 50179268 intron variant T/A snv 0.13 1
rs3116602
DLEU1 ; DLEU7
13 50537219 intron variant T/G snv 0.15 1
rs806352
DLEU1
13 50289783 intron variant T/G snv 0.49 1
rs471315
DLEU1
13 50387357 intron variant C/G;T snv 1
rs157170
DLEU1
13 50508319 intron variant A/G snv 0.71 1
rs3118917
DLEU7 ; DLEU1
13 50571933 intron variant C/A;T snv 3.9E-02 1
rs3118905
DLEU1 ; DLEU7
13 50531198 intron variant G/A snv 0.21 1
rs143794540
DLEU1
13 50277750 intron variant A/G snv 5.4E-03 1
rs3118906
DLEU1 ; DLEU7
13 50532652 intron variant G/A snv 0.21 1
rs3118077
LOC107984567 ; DLEU7 ; DLEU1
13 50728174 intron variant G/A snv 0.74 1
rs3116614
DLEU7 ; DLEU1
13 50576594 intron variant A/C snv 0.24 1
rs41308558
DLEU1
13 50157231 non coding transcript exon variant T/A;C;G snv 1