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: 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: rs10510732
rs10510732 		1 1.000 0.160 3 41965847 upstream gene variant G/A snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs10510733
rs10510733 		1 1.000 0.160 3 41967700 intergenic variant T/C snv 0.13 0.700 1.000 1 2011 2011
dbSNP: rs1057519933
rs1057519933
PIK3CA
11 0.790 0.240 3 179199156 missense variant A/G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519934
rs1057519934
PIK3CA
11 0.790 0.240 3 179199158 missense variant G/C snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519935
rs1057519935
PIK3CA
11 0.790 0.240 3 179199157 missense variant A/G snv 0.700 1.000 1 2016 2016
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: rs10936600
rs10936600
LRRC34
1 1.000 0.160 3 169796797 missense variant A/T snv 0.29 0.21 0.700 1.000 1 2016 2016
dbSNP: rs10936601
rs10936601
LRRC34
2 1.000 0.160 3 169810661 intron variant C/T snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs10936602
rs10936602
LRRIQ4
3 0.882 0.240 3 169818849 upstream gene variant T/C snv 0.26 0.700 1.000 1 2013 2013
dbSNP: rs10936603
rs10936603
LRRIQ4
1 1.000 0.160 3 169827864 intron variant G/A;T snv 0.700 1.000 1 2013 2013
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
dbSNP: rs111708447
rs111708447
ULK4
1 1.000 0.160 3 41768091 intron variant G/A snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs111821658
rs111821658
ULK4
1 1.000 0.160 3 41828974 intron variant C/G snv 0.23 0.700 1.000 1 2011 2011
dbSNP: rs111877184
rs111877184
ULK4
1 1.000 0.160 3 41775181 intron variant G/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs111967505
rs111967505
ULK4
1 1.000 0.160 3 41831665 intron variant C/T snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs112059754
rs112059754
ULK4
1 1.000 0.160 3 41822633 intron variant C/A;G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs112071272
rs112071272
ULK4
1 1.000 0.160 3 41781871 intron variant G/A snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs112245154
rs112245154
ULK4
1 1.000 0.160 3 41909028 intron variant G/T snv 0.13 0.700 1.000 1 2011 2011