Gene: SLC26A4 ×
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: rs1554355011
rs1554355011
SLC26A4
2 1.000 0.120 7 107674944 splice acceptor variant G/A snv 0.700 0
dbSNP: rs1554360358
rs1554360358
SLC26A4
3 0.925 0.160 7 107698076 missense variant A/C snv 0.700 0
dbSNP: rs1562835480
rs1562835480
SLC26A4
2 1.000 0.120 7 107694457 stop gained A/T snv 0.700 0
dbSNP: rs192366176
rs192366176
SLC26A4
4 0.925 0.160 7 107700180 splice region variant G/A snv 8.0E-06 1.4E-05 0.700 0
dbSNP: rs200455203
rs200455203
SLC26A4
4 0.925 0.160 7 107701998 missense variant G/C snv 8.0E-06 1.4E-05 0.700 0
dbSNP: rs201562855
rs201562855
SLC26A4
4 0.925 0.160 7 107690148 missense variant A/T snv 4.0E-06 0.700 0
dbSNP: rs201660407
rs201660407
SLC26A4
3 0.925 0.160 7 107690236 missense variant A/C;G snv 8.0E-06; 1.2E-05 0.700 0
dbSNP: rs371544695
rs371544695
SLC26A4 ; SLC26A4-AS1
2 1.000 0.120 7 107661750 stop gained G/C;T snv 2.7E-05 0.700 0
dbSNP: rs747076316
rs747076316
SLC26A4
3 0.925 0.160 7 107694622 stop gained C/A;G;T snv 2.0E-05 2.1E-05 0.700 0
dbSNP: rs749013429
rs749013429
SLC26A4
2 1.000 0.120 7 107702030 missense variant C/A;T snv 2.4E-05; 4.0E-06 0.700 0
dbSNP: rs752807925
rs752807925
SLC26A4
3 0.925 0.160 7 107704382 stop gained C/T snv 1.3E-05 0.700 0
dbSNP: rs763006761
rs763006761
SLC26A4
3 0.925 0.160 7 107700135 missense variant A/G snv 1.6E-05 0.700 0
dbSNP: rs767255075
rs767255075
SLC26A4
1 7 107700161 missense variant T/C;G snv 1.2E-05; 8.0E-06 0.700 0
dbSNP: rs786204474
rs786204474
SLC26A4
3 0.925 0.160 7 107689130 missense variant C/T snv 7.0E-06 0.700 0
dbSNP: rs786204739
rs786204739
SLC26A4
3 0.925 0.160 7 107698083 missense variant T/G snv 0.700 0