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: rs397515404
rs397515404
KCNT1
2 0.925 9 135768848 missense variant G/A snv 0.800 1.000 11 2012 2017
dbSNP: rs397515403
rs397515403
KCNT1
2 0.925 9 135779429 missense variant G/A snv 0.800 1.000 10 2012 2017
dbSNP: rs587777264
rs587777264
KCNT1
2 0.925 9 135759686 missense variant G/A snv 0.800 1.000 9 2012 2017
dbSNP: rs397515402
rs397515402
KCNT1
2 0.925 9 135765706 missense variant G/A snv 0.800 1.000 7 2012 2017
dbSNP: rs370521183
rs370521183
KCNT1
1 1.000 9 135775346 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 0.800 1.000 6 2012 2017
dbSNP: rs1424788778
rs1424788778
KCNT1 ; LOC107987139
1 1.000 9 135784078 missense variant G/A snv 0.700 1.000 6 2012 2017
dbSNP: rs397515406
rs397515406
KCNT1
2 0.925 9 135777374 missense variant T/C snv 0.700 1.000 6 2012 2017
dbSNP: rs397515407
rs397515407
KCNT1
2 0.925 9 135765188 missense variant G/A snv 0.700 1.000 6 2012 2016
dbSNP: rs886043455
rs886043455
KCNT1 ; LOC107987139
2 0.925 9 135784031 missense variant G/A;T snv 0.700 1.000 3 2015 2017
dbSNP: rs866242631
rs866242631
KCNT1
2 0.925 9 135768847 missense variant C/A;T snv 0.700 1.000 2 2012 2014
dbSNP: rs1057519544
rs1057519544
KCNT1
1 1.000 9 135779468 missense variant A/G snv 0.700 0
dbSNP: rs1060503696
rs1060503696
KCNT1
2 0.925 9 135778780 missense variant T/G snv 0.700 0
dbSNP: rs1185192267
rs1185192267
KCNT1
1 1.000 9 135770420 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs1554774322
rs1554774322
KCNT1
1 1.000 9 135768833 missense variant A/T snv 0.700 0
dbSNP: rs752514808
rs752514808
KCNT1
2 0.925 9 135765061 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 0.700 0
dbSNP: rs886041691
rs886041691
KCNT1
2 0.925 0.080 9 135769982 missense variant A/G snv 0.700 0