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: rs1206069342
rs1206069342
KCNG4
1 1.000 0.080 16 84237426 missense variant G/T snv 0.010 1.000 1 2017 2017
dbSNP: rs34787244
rs34787244
KCNG4
1 1.000 0.080 16 84222663 missense variant C/T snv 1.7E-03 1.9E-03 0.010 1.000 1 2017 2017
dbSNP: rs61740169
rs61740169
ERC1
1 1.000 0.080 12 1027951 missense variant G/C snv 1.5E-03 5.8E-04 0.010 1.000 1 2017 2017