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: rs1135401955
rs1135401955
KCNQ5
1 1.000 6 73003943 missense variant T/G snv 0.800 0
dbSNP: rs1135401956
rs1135401956
KCNQ5
1 1.000 6 73105359 missense variant C/A snv 0.800 0
dbSNP: rs1135401957
rs1135401957
KCNQ5
1 1.000 6 73133459 missense variant G/T snv 0.800 0
dbSNP: rs1135401958
rs1135401958
KCNQ5
1 1.000 6 73111384 missense variant C/G snv 0.800 0