Gene: DLEU1 ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs3118905
rs3118905
DLEU1 ; DLEU7
2 13 50531198 intron variant G/A snv 0.21 0.700 1.000 3 2010 2019
dbSNP: rs3118906
rs3118906
DLEU1 ; DLEU7
2 13 50532652 intron variant G/A snv 0.21 0.700 1.000 3 2013 2019
dbSNP: rs3116602
rs3116602
DLEU1 ; DLEU7
2 13 50537219 intron variant T/G snv 0.15 0.700 1.000 2 2008 2019
dbSNP: rs1239704
rs1239704
DLEU1 ; DLEU7
1 13 50578475 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1239948
rs1239948
DLEU1 ; DLEU7
3 13 50532386 intron variant A/T snv 0.59 0.700 1.000 1 2017 2017
dbSNP: rs143794540
rs143794540
DLEU1
1 13 50277750 intron variant A/G snv 5.4E-03 0.700 1.000 1 2019 2019
dbSNP: rs1568672
rs1568672
DLEU1
1 13 50179268 intron variant T/A snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs157170
rs157170
DLEU1
1 13 50508319 intron variant A/G snv 0.71 0.700 1.000 1 2017 2017
dbSNP: rs2687950
rs2687950
DLEU1
1 13 50144332 intron variant C/T snv 0.20 0.700 1.000 1 2014 2014
dbSNP: rs2812208
rs2812208
DLEU1
5 13 50132951 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs3116614
rs3116614
DLEU1 ; DLEU7
1 13 50576594 intron variant A/C snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs3118077
rs3118077
DLEU1 ; DLEU7 ; LOC107984567
1 13 50728174 intron variant G/A snv 0.74 0.700 1.000 1 2019 2019
dbSNP: rs3118914
rs3118914
DLEU1 ; DLEU7
2 13 50542765 intron variant G/T snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs3118917
rs3118917
DLEU1 ; DLEU7
1 13 50571933 intron variant C/A;T snv 3.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs386363597
rs386363597
DLEU1 ; DLEU7
1 13 50657252 intron variant -/C delins 1.4E-05 0.700 1.000 1 2017 2017
dbSNP: rs41284816
rs41284816
DLEU2 ; DLEU1
2 13 50081853 non coding transcript exon variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs41308558
rs41308558
DLEU1
1 13 50157231 non coding transcript exon variant T/A;C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs471315
rs471315
DLEU1
1 13 50387357 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs475883
rs475883
DLEU1 ; DLEU7
1 13 50599596 intron variant G/C snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs74788384
rs74788384
DLEU1
1 13 50158288 intron variant A/G snv 7.5E-03 0.700 1.000 1 2019 2019
dbSNP: rs806352
rs806352
DLEU1
1 13 50289783 intron variant T/G snv 0.49 0.700 1.000 1 2017 2017
dbSNP: rs978332
rs978332
DLEU1 ; DLEU7
1 13 50562603 intron variant C/T snv 0.69 0.700 1.000 1 2017 2017