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: rs10459648
rs10459648
ARID3B
1 1.000 0.080 15 74573099 intron variant C/T snv 0.25; 4.0E-06 0.25 0.700 1.000 1 2016 2016
dbSNP: rs10905359
rs10905359 		1 1.000 0.080 10 8407928 intron variant C/A snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs11263613
rs11263613 		1 1.000 0.080 11 69846566 regulatory region variant G/A snv 4.2E-02 0.700 1.000 1 2016 2016
dbSNP: rs13089920
rs13089920 		1 1.000 0.080 3 78503082 intergenic variant A/G snv 0.28 0.700 1.000 1 2016 2016
dbSNP: rs17090300
rs17090300
LINC00392 ; LINC00393 ; LOC107984024
1 1.000 0.080 13 73583314 intron variant G/A snv 6.7E-02 0.700 1.000 1 2016 2016
dbSNP: rs17802111
rs17802111
LOC101926974
1 1.000 0.080 2 46282518 intergenic variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs3754648
rs3754648
AGAP1
1 1.000 0.080 2 236112702 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs3923380
rs3923380
SHROOM3
1 1.000 0.080 4 76547441 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs4750407
rs4750407
FRMD4A
1 1.000 0.080 10 13753471 intron variant A/G snv 0.21 0.700 1.000 1 2016 2016
dbSNP: rs7420812
rs7420812
PARD3B
1 1.000 0.080 2 205570985 intron variant T/C snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs754423
rs754423
NID2
1 1.000 0.080 14 52060469 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs869025667
rs869025667
VHL
6 0.827 0.200 3 10149916 missense variant T/C snv 0.010 1.000 1 2014 2014