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: rs137852608
rs137852608
CNGA3
1 1.000 0.120 2 98396398 missense variant C/T snv 4.0E-05 4.2E-05 0.800 1.000 13 1998 2017
dbSNP: rs104893614
rs104893614
CNGA3
2 0.925 0.120 2 98396018 missense variant G/A snv 6.4E-05 9.8E-05 0.800 1.000 10 1998 2015
dbSNP: rs104893612
rs104893612
CNGA3
1 1.000 0.120 2 98389696 missense variant C/T snv 1.6E-05 7.0E-06 0.800 1.000 8 1998 2015
dbSNP: rs104893613
rs104893613
CNGA3
2 0.925 0.120 2 98396017 missense variant C/T snv 9.9E-05 2.1E-05 0.800 1.000 8 1998 2015
dbSNP: rs104893616
rs104893616
CNGA3
1 1.000 0.120 2 98396042 missense variant C/G snv 0.800 1.000 8 1998 2015
dbSNP: rs104893617
rs104893617
CNGA3
2 0.925 0.120 2 98396811 missense variant C/A;T snv 1.5E-04; 4.4E-05 0.800 1.000 8 1998 2015
dbSNP: rs104893619
rs104893619
CNGA3
3 0.882 0.120 2 98396755 missense variant G/A snv 6.8E-05 3.5E-05 0.800 1.000 8 1998 2015
dbSNP: rs104893620
rs104893620
CNGA3
6 0.851 0.120 2 98395999 missense variant C/T snv 9.5E-05 7.0E-05 0.800 1.000 8 1998 2015
dbSNP: rs104893621
rs104893621
CNGA3
3 0.882 0.120 2 98396476 missense variant C/T snv 9.6E-05 6.3E-05 0.800 1.000 8 1998 2015
dbSNP: rs141386891
rs141386891
CNGA3
3 0.882 0.120 2 98396449 missense variant C/T snv 4.0E-04 4.1E-04 0.710 1.000 1 2019 2019
dbSNP: rs104893615
rs104893615
CNGA3
1 1.000 0.120 2 98396839 missense variant G/A snv 1.4E-04 1.2E-04 0.700 1.000 8 1998 2015
dbSNP: rs138958917
rs138958917
CNGA3
2 0.925 0.120 2 98391964 missense variant C/G;T snv 3.6E-05; 7.6E-05 0.700 1.000 8 1998 2015
dbSNP: rs1464167194
rs1464167194
CNGA3
1 1.000 0.120 2 98396284 missense variant C/T snv 8.0E-06 0.700 1.000 8 1998 2015
dbSNP: rs1553450734
rs1553450734
CNGA3
2 0.925 0.120 2 98396387 missense variant T/C snv 0.700 1.000 8 1998 2015
dbSNP: rs201747279
rs201747279
CNGA3
1 1.000 0.120 2 98396864 missense variant C/T snv 1.6E-04 1.9E-04 0.700 1.000 8 1998 2015
dbSNP: rs201782746
rs201782746
CNGA3
1 1.000 0.120 2 98396876 missense variant G/A;T snv 1.6E-05 2.8E-05 0.700 1.000 8 1998 2015
dbSNP: rs373954146
rs373954146
CNGA3
1 1.000 0.120 2 98396582 missense variant A/G;T snv 1.2E-05 0.700 1.000 8 1998 2015
dbSNP: rs374258471
rs374258471
CNGA3
1 1.000 0.120 2 98395948 missense variant G/A;C snv 2.4E-05; 8.0E-06 0.700 1.000 8 1998 2015
dbSNP: rs552069173
rs552069173
CNGA3
2 1.000 0.120 2 98396858 missense variant G/A snv 7.6E-05 3.5E-05 0.700 1.000 8 1998 2015
dbSNP: rs747447519
rs747447519
CNGA3
1 1.000 0.120 2 98389693 missense variant A/T snv 9.5E-05 1.4E-05 0.700 1.000 8 1998 2015
dbSNP: rs749842881
rs749842881
CNGA3
1 1.000 0.120 2 98396485 missense variant C/T snv 2.0E-05 7.0E-06 0.700 1.000 8 1998 2015
dbSNP: rs761554853
rs761554853
CNGA3
1 1.000 0.120 2 98391869 missense variant G/A;C snv 1.2E-05; 4.0E-06 0.700 1.000 8 1998 2015
dbSNP: rs762668060
rs762668060
CNGA3
1 1.000 0.120 2 98391965 missense variant G/A snv 4.4E-05 2.1E-05 0.700 1.000 8 1998 2015
dbSNP: rs762773298
rs762773298
CNGA3
1 1.000 0.120 2 98389721 stop gained G/A;T snv 8.0E-06; 4.0E-06 0.700 1.000 8 1998 2015
dbSNP: rs763041373
rs763041373
CNGA3
1 1.000 0.120 2 98396938 missense variant G/A snv 8.0E-06 7.0E-06 0.700 1.000 8 1998 2015