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: rs121908354
rs121908354
CDH23
4 0.882 0.240 10 71570884 missense variant C/T snv 4.0E-05 7.0E-06 0.800 1.000 11 2001 2015
dbSNP: rs111033271
rs111033271
CDH23
2 0.925 0.200 10 71793370 missense variant G/A snv 9.2E-05 9.8E-05 0.800 1.000 10 2001 2014
dbSNP: rs121908348
rs121908348
CDH23 ; MIR7152
1 1.000 0.120 10 71791215 missense variant G/A snv 4.0E-06 0.800 1.000 8 2001 2014
dbSNP: rs121908349
rs121908349
CDH23
1 1.000 0.120 10 71793532 missense variant G/A;T snv 8.0E-06; 4.0E-06 0.800 1.000 8 2001 2014
dbSNP: rs121908351
rs121908351
CDH23 ; C10orf105
1 1.000 0.120 10 71732292 missense variant G/A snv 4.1E-06 0.800 1.000 8 2001 2014
dbSNP: rs121908352
rs121908352
CDH23
1 1.000 0.120 10 71785051 missense variant T/C snv 0.800 1.000 8 2001 2014
dbSNP: rs1554871816
rs1554871816
CDH23
2 1.000 0.120 10 71777711 missense variant A/C snv 0.800 1.000 8 2001 2014
dbSNP: rs750880909
rs750880909
CDH23 ; MIR7152
2 1.000 0.120 10 71791167 missense variant C/T snv 2.4E-05 2.1E-05 0.800 1.000 8 2001 2014
dbSNP: rs756147087
rs756147087
CDH23
2 1.000 0.120 10 71705043 missense variant G/A snv 3.2E-05 9.1E-05 0.800 1.000 8 2001 2014
dbSNP: rs771766431
rs771766431
CDH23
1 1.000 0.120 10 71706911 missense variant G/A snv 1.4E-05 0.710 1.000 1 2018 2018
dbSNP: rs121908355
rs121908355
CDH23
1 1.000 0.120 10 71615573 missense variant G/A;C snv 8.0E-06 0.700 1.000 8 2001 2014
dbSNP: rs201536811
rs201536811
CDH23
1 1.000 0.120 10 71709169 missense variant C/A;T snv 4.0E-06; 4.8E-04 0.700 1.000 8 2001 2014
dbSNP: rs202052174
rs202052174
CDH23
1 1.000 0.120 10 71803371 missense variant G/A snv 6.7E-04 5.8E-04 0.700 1.000 8 2001 2014
dbSNP: rs573737471
rs573737471
CDH23
1 1.000 0.120 10 71741832 missense variant G/A;C snv 8.2E-06; 4.1E-06 0.700 1.000 8 2001 2014
dbSNP: rs752937051
rs752937051
CDH23
1 1.000 0.120 10 71809946 missense variant T/A snv 0.700 1.000 8 2001 2014
dbSNP: rs760879110
rs760879110
CDH23
1 1.000 0.120 10 71800666 missense variant C/A;T snv 4.0E-06; 8.0E-06 0.700 1.000 8 2001 2014
dbSNP: rs762247872
rs762247872
CDH23 ; C10orf105
1 1.000 0.120 10 71732374 missense variant C/T snv 1.8E-05 9.1E-05 0.700 1.000 8 2001 2014
dbSNP: rs767928788
rs767928788
CDH23
1 1.000 0.120 10 71646607 missense variant T/A;C snv 4.0E-06 0.700 1.000 8 2001 2014
dbSNP: rs778204574
rs778204574
CDH23
1 1.000 0.120 10 71741859 missense variant G/A snv 2.1E-05 1.4E-05 0.700 1.000 8 2001 2014
dbSNP: rs1057519500
rs1057519500
CDH23
1 1.000 0.120 10 71566790 missense variant G/A snv 4.0E-06 7.0E-06 0.700 0
dbSNP: rs1060499788
rs1060499788
CDH23
1 1.000 0.120 10 71570848 missense variant A/T snv 0.700 0
dbSNP: rs1060499789
rs1060499789
CDH23
1 1.000 0.120 10 71785667 missense variant G/A snv 0.700 0
dbSNP: rs1060499790
rs1060499790
CDH23
1 1.000 0.120 10 71807302 missense variant T/C snv 0.700 0
dbSNP: rs1060499791
rs1060499791
CDH23
2 1.000 0.120 10 71617295 missense variant C/T snv 0.700 0
dbSNP: rs1060499792
rs1060499792
CDH23
1 1.000 0.120 10 71677616 missense variant C/T snv 0.700 0