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: rs121434408
rs121434408
GLE1 ; LOC101929270
1 1.000 0.120 9 128538058 missense variant G/A snv 1.6E-05 2.1E-05 0.800 1.000 1 2008 2008
dbSNP: rs121434409
rs121434409
GLE1 ; LOC101929270
2 0.925 0.120 9 128541124 missense variant T/C snv 3.6E-05 2.1E-05 0.800 1.000 1 2008 2008
dbSNP: rs121434407
rs121434407
GLE1 ; LOC101929270
5 0.882 0.120 9 128536414 missense variant G/A snv 2.7E-04 9.8E-05 0.710 1.000 1 2018 2018
dbSNP: rs1336481358
rs1336481358
GLE1 ; LOC101929270
1 1.000 0.120 9 128539614 splice acceptor variant A/G snv 8.0E-06 7.0E-06 0.700 0
dbSNP: rs1564162129
rs1564162129
GLE1 ; LOC101929270
1 1.000 0.120 9 128541151 missense variant C/T snv 0.700 0
dbSNP: rs386833693
rs386833693
GLE1
2 0.925 0.120 9 128522658 intron variant A/G;T snv 1.5E-05; 9.7E-04 0.700 0
dbSNP: rs765269946
rs765269946
GLE1 ; LOC101929270
1 1.000 0.120 9 128536458 missense variant C/T snv 3.6E-05 2.8E-05 0.700 0