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: rs1202784860
rs1202784860
DYNC2H1
1 1.000 0.080 11 103177653 missense variant T/A;C snv 0.700 1.000 4 2009 2013
dbSNP: rs1265669915
rs1265669915
DYNC2H1
1 1.000 0.080 11 103199307 missense variant T/C snv 0.700 1.000 4 2009 2013
dbSNP: rs1278825521
rs1278825521
DYNC2H1
1 1.000 0.080 11 103197942 missense variant A/G snv 5.4E-06 0.700 1.000 4 2009 2013
dbSNP: rs137853025
rs137853025
DYNC2H1
1 1.000 0.080 11 103177652 missense variant A/T snv 0.800 1.000 4 2009 2013
dbSNP: rs137853028
rs137853028
DYNC2H1
1 1.000 0.080 11 103155476 missense variant T/C snv 3.3E-05 2.1E-05 0.800 1.000 4 2009 2013
dbSNP: rs137853030
rs137853030
DYNC2H1
1 1.000 0.080 11 103125197 missense variant C/T snv 4.0E-06 7.0E-06 0.800 1.000 4 2009 2013
dbSNP: rs137853033
rs137853033
DYNC2H1
1 1.000 0.080 11 103163146 missense variant A/G snv 0.800 1.000 4 2009 2013
dbSNP: rs137853034
rs137853034
DYNC2H1
1 1.000 0.080 11 103189761 missense variant G/T snv 0.800 1.000 4 2009 2013
dbSNP: rs137853035
rs137853035
DYNC2H1
1 1.000 0.080 11 103177640 missense variant A/G snv 0.800 1.000 4 2009 2013
dbSNP: rs374073337
rs374073337
DYNC2H1
1 1.000 0.080 11 103120964 missense variant C/T snv 2.2E-04 5.2E-04 0.700 1.000 4 2009 2013
dbSNP: rs397514635
rs397514635
DYNC2H1
1 1.000 0.080 11 103199373 missense variant G/A snv 1.2E-05 1.4E-05 0.800 1.000 4 2009 2013
dbSNP: rs397514636
rs397514636
DYNC2H1
1 1.000 0.080 11 103191565 missense variant C/T snv 0.800 1.000 4 2009 2013
dbSNP: rs754753584
rs754753584
DYNC2H1
1 1.000 0.080 11 103307754 missense variant C/A;T snv 4.2E-06; 1.7E-05 0.700 1.000 4 2009 2013
dbSNP: rs763571787
rs763571787
DYNC2H1
1 1.000 0.080 11 103158974 missense variant G/A snv 4.0E-06 7.0E-06 0.700 1.000 4 2009 2013
dbSNP: rs781326398
rs781326398
DYNC2H1
1 1.000 0.080 11 103191521 missense variant G/A snv 3.0E-05 4.9E-05 0.700 1.000 4 2009 2013
dbSNP: rs755883373
rs755883373
DYNC2H1
1 1.000 0.080 11 103135727 stop gained C/G;T snv 4.1E-06; 4.1E-06 0.700 1.000 1 2009 2009
dbSNP: rs759549373
rs759549373
DYNC2H1
4 0.925 0.080 11 103253342 missense variant G/A;T snv 6.0E-05; 4.0E-06 0.700 1.000 1 2016 2016
dbSNP: rs1043384862
rs1043384862
DYNC2H1
1 1.000 0.080 11 103165911 missense variant C/T snv 0.700 0
dbSNP: rs1060501431
rs1060501431
DYNC2H1
1 1.000 0.080 11 103209878 missense variant A/G snv 9.0E-06 7.0E-06 0.700 0
dbSNP: rs1214801816
rs1214801816
DYNC2H1
1 1.000 0.080 11 103199458 missense variant C/G;T snv 7.0E-06 0.700 0
dbSNP: rs1243999036
rs1243999036
DYNC2H1
1 1.000 0.080 11 103184992 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs1261505725
rs1261505725
DYNC2H1
2 0.925 0.080 11 103245376 splice donor variant T/G snv 5.0E-06 2.1E-05 0.700 0
dbSNP: rs1322077043
rs1322077043
DYNC2H1
1 1.000 0.080 11 103120459 missense variant A/G snv 0.700 0
dbSNP: rs1322884865
rs1322884865
DYNC2H1
1 1.000 0.080 11 103187558 missense variant C/T snv 8.1E-06 7.0E-06 0.700 0
dbSNP: rs1332318318
rs1332318318
DYNC2H1
1 1.000 0.080 11 103181796 stop gained G/A;T snv 0.700 0