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: rs397515476
rs397515476
KCND3
1 1.000 0.080 1 111981673 missense variant T/C;G snv 0.800 1.000 4 2010 2018
dbSNP: rs797045634
rs797045634
KCND3
1 1.000 0.080 1 111981693 missense variant C/A snv 0.800 1.000 4 2010 2018
dbSNP: rs397515477
rs397515477
KCND3
1 1.000 0.080 1 111787094 missense variant C/T snv 0.700 1.000 3 2012 2018
dbSNP: rs397515478
rs397515478
KCND3
1 1.000 0.080 1 111787044 missense variant C/T snv 0.700 1.000 3 2012 2018
dbSNP: rs1057519453
rs1057519453
KCND3
1 1.000 0.080 1 111787060 missense variant A/G snv 0.700 0
dbSNP: rs1057521793
rs1057521793
KCND3
1 1.000 0.080 1 111787102 missense variant C/T snv 0.700 0
dbSNP: rs397515475
rs397515475
KCND3
1 1.000 0.080 1 111982045 inframe deletion AAG/- delins 0.700 0