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: rs104894228
rs104894228
HRAS ; LRRC56
48 0.605 0.560 11 534286 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs104894229
rs104894229
HRAS ; LRRC56
73 0.564 0.600 11 534289 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs104894230
rs104894230
HRAS ; LRRC56
73 0.564 0.600 11 534288 missense variant C/A;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs104894231
rs104894231
HRAS ; LRRC56
9 0.776 0.360 11 533467 missense variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs104894340
rs104894340
CDK4
5 0.827 0.200 12 57751647 missense variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1050976
rs1050976
IRF4
4 0.851 0.280 6 408079 3 prime UTR variant C/T snv 0.37 0.700 1.000 1 2018 2018
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: rs1057519877
rs1057519877
B2M ; PATL2
10 0.763 0.280 15 44711549 start lost G/A snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519879
rs1057519879
B2M ; PATL2
10 0.763 0.280 15 44711548 start lost T/C;G snv 0.700 1.000 1 2016 2016
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: rs1057519977
rs1057519977
TP53
13 0.763 0.360 17 7675189 missense variant G/C snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519978
rs1057519978
TP53
12 0.763 0.360 17 7675191 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519981
rs1057519981
TP53
22 0.689 0.440 17 7674251 missense variant A/C;G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519983
rs1057519983
TP53
16 0.724 0.360 17 7673797 missense variant A/G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057519996
rs1057519996
TP53
19 0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs1057520007
rs1057520007
TP53
21 0.701 0.440 17 7674917 missense variant T/A;C;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