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: rs121909088
rs121909088
DNM2
3 0.925 0.080 19 10819992 missense variant A/G snv 0.800 1.000 2 2005 2009
dbSNP: rs121909093
rs121909093
DNM2
2 0.925 0.080 19 10812315 missense variant G/A;T snv 0.800 1.000 2 2007 2008
dbSNP: rs267606772
rs267606772
DNM2
3 0.925 0.080 19 10793799 missense variant G/A snv 0.800 1.000 2 2007 2008
dbSNP: rs121909092
rs121909092
DNM2
4 0.882 0.120 19 10793829 missense variant G/A snv 0.700 1.000 18 2005 2015
dbSNP: rs121909090
rs121909090
DNM2
3 0.882 0.120 19 10793832 missense variant C/T snv 7.0E-06 0.700 1.000 8 2005 2017
dbSNP: rs121909095
rs121909095
DNM2
3 0.882 0.120 19 10823862 missense variant C/G;T snv 0.700 1.000 8 2007 2015
dbSNP: rs587783595
rs587783595
DNM2
3 0.882 0.120 19 10812271 missense variant G/A;T snv 0.700 1.000 8 2010 2016
dbSNP: rs121909089
rs121909089
DNM2
3 0.882 0.120 19 10793833 missense variant G/A;T snv 0.700 1.000 7 2005 2017
dbSNP: rs121909091
rs121909091
DNM2
4 0.851 0.120 19 10798543 missense variant C/T snv 0.700 1.000 6 2005 2016
dbSNP: rs121909094
rs121909094
DNM2
1 1.000 0.080 19 10820017 missense variant T/A snv 0.700 1.000 2 2007 2008
dbSNP: rs1555715869
rs1555715869
DNM2
2 0.925 0.120 19 10823859 missense variant C/A snv 0.700 1.000 1 2010 2010
dbSNP: rs746903992
rs746903992
DNM2
1 1.000 0.080 19 10802328 missense variant C/A;G;T snv 8.0E-06; 1.2E-05 0.700 0
dbSNP: rs864309705
rs864309705
DNM2
1 1.000 0.080 19 10793748 missense variant G/A snv 0.700 0