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: 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: rs10180663
rs10180663
DTNB
1 1.000 0.160 2 25410373 intron variant T/A;C;G snv 0.700 1.000 1 2013 2013
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: rs1034447
rs1034447
LOC105378110
1 1.000 0.160 6 164192425 intergenic variant C/T snv 0.24 0.700 1.000 1 2016 2016
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: rs1045433
rs1045433
TRNT1 ; CRBN
1 1.000 0.160 3 3149742 non coding transcript exon variant T/C snv 0.15 0.010 1.000 1 2016 2016
dbSNP: rs10485986
rs10485986
DNAH11
1 1.000 0.160 7 21867059 intron variant C/T snv 0.32 0.700 1.000 1 2011 2011
dbSNP: rs1049633
rs1049633
DDR1
1 1.000 0.160 6 30899750 3 prime UTR variant G/A snv 7.6E-02 0.010 1.000 1 2017 2017
dbSNP: rs10509328
rs10509328
LOC105378351
1 1.000 0.160 10 71007652 intron variant T/A;C snv 0.800 1.000 1 2013 2013
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: 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: rs10936603
rs10936603
LRRIQ4
1 1.000 0.160 3 169827864 intron variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs11064392
rs11064392
CD4
1 1.000 0.160 12 6789226 intron variant A/G snv 0.14 0.010 1.000 1 2010 2010
dbSNP: rs11086029
rs11086029
KLF2
1 1.000 0.160 19 16327850 3 prime UTR variant T/A snv 0.78 0.700 1.000 1 2018 2018
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