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: rs137853260
rs137853260
1 1.000 0.200 X 129569296 missense variant G/A snv 0.800 1.000 10 1997 2011
dbSNP: rs137853261
rs137853261
1 1.000 0.200 X 129569369 missense variant C/G snv 0.800 1.000 10 1997 2011
dbSNP: rs137853263
rs137853263
2 0.925 0.200 X 129562396 missense variant C/A;T snv 0.700 1.000 10 1997 2011
dbSNP: rs137853828
rs137853828
1 1.000 0.200 X 129560552 missense variant T/C snv 0.700 1.000 10 1997 2011
dbSNP: rs137853829
rs137853829
1 1.000 0.200 X 129560648 missense variant T/C snv 0.700 1.000 10 1997 2011
dbSNP: rs137853830
rs137853830
1 1.000 0.200 X 129561184 missense variant A/G snv 0.700 1.000 10 1997 2011
dbSNP: rs137853831
rs137853831
1 1.000 0.200 X 129562453 missense variant C/A;T snv 1.1E-05; 5.5E-06 0.700 1.000 10 1997 2011
dbSNP: rs137853832
rs137853832
1 1.000 0.200 X 129562624 missense variant G/T snv 0.700 1.000 10 1997 2011
dbSNP: rs137853834
rs137853834
1 1.000 0.200 X 129562657 missense variant T/G snv 0.700 1.000 10 1997 2011
dbSNP: rs137853835
rs137853835
1 1.000 0.200 X 129562659 missense variant A/T snv 0.700 1.000 10 1997 2011
dbSNP: rs137853836
rs137853836
1 1.000 0.200 X 129562663 missense variant C/T snv 0.700 1.000 10 1997 2011
dbSNP: rs137853837
rs137853837
1 1.000 0.200 X 129562783 missense variant A/G snv 0.700 1.000 10 1997 2011
dbSNP: rs137853838
rs137853838
1 1.000 0.200 X 129565878 missense variant G/A snv 0.700 1.000 10 1997 2011
dbSNP: rs137853839
rs137853839
1 1.000 0.200 X 129567266 missense variant C/G snv 0.700 1.000 10 1997 2011
dbSNP: rs137853840
rs137853840
1 1.000 0.200 X 129567299 missense variant G/A snv 0.700 1.000 10 1997 2011
dbSNP: rs137853841
rs137853841
1 1.000 0.200 X 129567300 missense variant A/G snv 0.700 1.000 10 1997 2011
dbSNP: rs137853842
rs137853842
1 1.000 0.200 X 129569292 missense variant G/C snv 0.700 1.000 10 1997 2011
dbSNP: rs137853843
rs137853843
1 1.000 0.200 X 129569304 missense variant T/C snv 0.700 1.000 10 1997 2011
dbSNP: rs137853844
rs137853844
1 1.000 0.200 X 129575956 missense variant C/A snv 0.700 1.000 10 1997 2011
dbSNP: rs137853845
rs137853845
1 1.000 0.200 X 129590236 missense variant T/G snv 0.700 1.000 10 1997 2011
dbSNP: rs137853847
rs137853847
1 1.000 0.200 X 129569335 missense variant A/G snv 0.700 1.000 10 1997 2011
dbSNP: rs137853848
rs137853848
1 1.000 0.200 X 129562665 missense variant C/T snv 0.700 1.000 10 1997 2011
dbSNP: rs137853849
rs137853849
1 1.000 0.200 X 129569320 missense variant T/A snv 0.700 1.000 10 1997 2011
dbSNP: rs137853850
rs137853850
1 1.000 0.200 X 129565879 missense variant A/G snv 0.700 1.000 10 1997 2011
dbSNP: rs137853851
rs137853851
1 1.000 0.200 X 129567285 missense variant T/C snv 0.700 1.000 10 1997 2011