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: rs121908928
rs121908928
COCH ; LOC100506071
2 1.000 0.120 14 30878834 missense variant G/A;T snv 8.0E-06 0.810 1.000 14 1998 2014
dbSNP: rs121908930
rs121908930
COCH ; LOC100506071
3 0.925 0.120 14 30878897 missense variant T/A;C snv 4.0E-06 0.810 1.000 14 1998 2014
dbSNP: rs121908932
rs121908932
COCH ; LOC100506071
2 0.925 0.120 14 30889763 missense variant G/A;T snv 0.800 1.000 14 1998 2014
dbSNP: rs121908927
rs121908927
COCH ; LOC100506071
1 1.000 0.120 14 30877686 missense variant T/C;G snv 8.0E-06 0.800 1.000 13 1998 2014
dbSNP: rs121908929
rs121908929
COCH ; LOC100506071
1 1.000 0.120 14 30878920 missense variant T/C snv 0.800 1.000 13 1998 2014
dbSNP: rs121908934
rs121908934
COCH ; LOC100506071
1 1.000 0.120 14 30889673 missense variant T/C snv 4.0E-06 7.0E-06 0.800 1.000 13 1998 2014
dbSNP: rs28938175
rs28938175
COCH ; LOC100506071
6 0.851 0.120 14 30877640 missense variant C/T snv 4.0E-06 0.710 1.000 1 2005 2005
dbSNP: rs121908931
rs121908931
COCH ; LOC100506071
1 1.000 0.120 14 30878926 missense variant G/A snv 0.700 1.000 13 1998 2014
dbSNP: rs756541797
rs756541797
COCH ; LOC100506071
1 1.000 0.120 14 30885985 missense variant C/T snv 9.1E-05 6.3E-05 0.700 0
dbSNP: rs878853226
rs878853226
COCH ; LOC100506071
1 1.000 0.120 14 30885994 missense variant C/T snv 0.700 0