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: rs192378817
rs192378817
MYO7A
1 11 77183146 missense variant C/A;T snv 3.9E-05 1.5E-04 0.700 0
dbSNP: rs201866631
rs201866631
USH1G
4 0.882 0.200 17 74920325 stop gained C/A;T snv 4.1E-06; 8.1E-06 0.700 0
dbSNP: rs367688416
rs367688416
PJVK
1 2 178454526 stop gained C/T snv 1.6E-05 1.4E-05 0.700 0
dbSNP: rs538027448
rs538027448
PJVK
1 2 178453567 stop gained C/G;T snv 4.0E-06 0.700 0
dbSNP: rs74315437
rs74315437
CLDN14 ; LOC105369301
2 1.000 21 36461442 missense variant A/G;T snv 4.0E-06; 2.0E-05 0.700 0
dbSNP: rs746667217
rs746667217
MYO7A
1 11 77205503 missense variant C/G;T snv 6.4E-05 2.1E-05 0.700 0
dbSNP: rs751242455
rs751242455
MYO7A
1 11 77204094 missense variant G/A;C snv 8.8E-06; 4.4E-05 0.700 0
dbSNP: rs755804651
rs755804651
GPSM2 ; AKNAD1
1 1 108896945 missense variant C/A snv 8.0E-06 7.0E-06 0.700 0
dbSNP: rs761261855
rs761261855
TMC1
1 9 72816175 missense variant C/G;T snv 1.2E-05 7.0E-06 0.700 0
dbSNP: rs762118583
rs762118583
CDH23 ; MIR7152
1 10 71791284 missense variant A/C snv 8.0E-06 7.0E-06 0.700 0
dbSNP: rs767797828
rs767797828
USH2A ; LOC105372918
1 1 216199777 stop gained G/A snv 4.0E-06 0.700 0
dbSNP: rs773851192
rs773851192
TMC1
1 9 72789302 stop gained G/A;C snv 4.0E-06 0.700 0