Gene: ULK4 ×
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: rs1052501
rs1052501
ULK4
2 0.925 0.160 3 41883906 missense variant C/G;T snv 0.80 0.810 1.000 3 2011 2014
dbSNP: rs2272007
rs2272007
ULK4
2 1.000 0.160 3 41954644 missense variant T/C snv 0.79 0.67 0.800 1.000 3 2011 2013
dbSNP: rs6599175
rs6599175
ULK4
1 1.000 0.160 3 41744517 intron variant T/C snv 0.32 0.800 1.000 3 2011 2013
dbSNP: rs6599192
rs6599192
ULK4
1 1.000 0.160 3 41950916 intron variant G/A snv 0.68 0.800 1.000 2 2011 2016
dbSNP: rs6763508
rs6763508
ULK4
4 0.851 0.160 3 41709497 intron variant T/C snv 0.30 0.800 1.000 2 2011 2017
dbSNP: rs73071352
rs73071352
ULK4
3 0.882 0.160 3 41786808 intron variant A/G snv 0.12 0.800 1.000 2 2011 2015
dbSNP: rs1125203
rs1125203
ULK4
1 1.000 0.160 3 41719403 intron variant T/C snv 0.33 0.700 1.000 2 2011 2013
dbSNP: rs17215589
rs17215589
ULK4
1 1.000 0.160 3 41789711 missense variant C/A;T snv 0.12 0.700 1.000 2 2011 2013
dbSNP: rs1994157
rs1994157
ULK4
1 1.000 0.160 3 41855990 intron variant G/A snv 0.18 0.700 1.000 2 2011 2013
dbSNP: rs2128835
rs2128835
ULK4
1 1.000 0.160 3 41821381 intron variant A/G snv 0.26 0.700 1.000 2 2011 2013
dbSNP: rs3774372
rs3774372
ULK4
4 1.000 0.160 3 41835922 missense variant T/C snv 0.17 0.18 0.700 1.000 2 2011 2013
dbSNP: rs1016669
rs1016669
ULK4
1 1.000 0.160 3 41852948 intron variant T/C snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs10212536
rs10212536
ULK4
1 1.000 0.160 3 41785534 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs1025646
rs1025646
ULK4
1 1.000 0.160 3 41712930 intron variant A/T snv 0.26 0.700 1.000 1 2011 2011
dbSNP: rs10452020
rs10452020
ULK4
1 1.000 0.160 3 41774459 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10452022
rs10452022
ULK4
1 1.000 0.160 3 41774550 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs10510729
rs10510729
ULK4
1 1.000 0.160 3 41790506 intron variant G/A snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs10510731
rs10510731
ULK4
1 1.000 0.160 3 41811818 intron variant C/T snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs10865914
rs10865914
ULK4
1 1.000 0.160 3 41878007 intron variant C/A;G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11129932
rs11129932
ULK4
1 1.000 0.160 3 41797275 intron variant C/A snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs11129935
rs11129935
ULK4
1 1.000 0.160 3 41943711 intron variant A/C snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs111304140
rs111304140
ULK4
1 1.000 0.160 3 41765000 intron variant G/A snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs111419796
rs111419796
ULK4
1 1.000 0.160 3 41935476 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs111465678
rs111465678
ULK4
1 1.000 0.160 3 41822913 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs111634789
rs111634789
ULK4
1 1.000 0.160 3 41829864 intron variant T/C;G snv 0.700 1.000 1 2011 2011