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: rs267601046
rs267601046
TTBK1 ; LOC105375064
1 1.000 0.040 6 43283303 missense variant C/T snv 0.700 0
dbSNP: rs267601191
rs267601191
EPHB4
1 1.000 0.040 7 100819817 missense variant G/A snv 0.700 0
dbSNP: rs267605306
rs267605306
PKN1
1 1.000 0.040 19 14446504 missense variant C/G;T snv 1.6E-05 0.700 0
dbSNP: rs369098292
rs369098292
TTN ; TTN-AS1
1 1.000 0.040 2 178572742 missense variant G/A snv 4.0E-06 1.4E-05 0.700 0
dbSNP: rs374713701
rs374713701
TTN ; TTN-AS1
1 1.000 0.040 2 178593660 missense variant C/A;T snv 4.0E-06; 8.1E-06 0.700 0
dbSNP: rs375422359
rs375422359
TTN ; TTN-AS1
1 1.000 0.040 2 178563634 missense variant C/T snv 2.4E-05 3.5E-05 0.700 0
dbSNP: rs55735910
rs55735910
PRKDC
1 1.000 0.040 8 47881444 missense variant G/A snv 1.4E-05 0.700 0
dbSNP: rs564777385
rs564777385
TTN
1 1.000 0.040 2 178800635 missense variant C/G;T snv 3.6E-05 0.700 0
dbSNP: rs764005465
rs764005465
TTN ; TTN-AS1
1 1.000 0.040 2 178572808 missense variant C/T snv 8.1E-06 0.700 0
dbSNP: rs779173667
rs779173667
PDGFRA
1 1.000 0.040 4 54290418 missense variant G/A snv 8.0E-06 1.4E-05 0.700 0
dbSNP: rs868224085
rs868224085
EPHA4
1 1.000 0.040 2 221482474 missense variant G/A snv 0.700 0
dbSNP: rs907102077
rs907102077
OGG1 ; CAMK1
1 1.000 0.040 3 9760752 missense variant G/A snv 0.700 0
dbSNP: rs121913377
rs121913377
BRAF
480 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 0.100 1.000 91 2004 2020
dbSNP: rs121913227
rs121913227
BRAF
31 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 0.090 1.000 9 2012 2018
dbSNP: rs1057519695
rs1057519695
NRAS
35 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 0.030 1.000 3 2015 2016
dbSNP: rs1057519834
rs1057519834
NRAS
31 0.658 0.480 1 114713908 missense variant TG/CT mnv 0.030 1.000 3 2015 2016
dbSNP: rs121913368
rs121913368
BRAF
2 0.925 0.040 7 140753345 missense variant AG/GA mnv 0.020 1.000 2 2012 2018