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: rs104894699
rs104894699
KCNC3
4 0.925 0.120 19 50323694 missense variant C/T snv 0.820 1.000 9 2006 2015
dbSNP: rs104894700
rs104894700
KCNC3
2 0.925 0.200 19 50323609 missense variant G/C;T snv 0.800 1.000 8 2006 2015
dbSNP: rs797044872
rs797044872
KCNC3
3 0.882 0.200 19 50323685 missense variant C/T snv 0.800 1.000 1 2010 2010
dbSNP: rs1460306526
rs1460306526
KCNC3
1 1.000 0.080 19 50323019 missense variant G/C snv 7.0E-06 0.700 1.000 7 2006 2015
dbSNP: rs549394447
rs549394447
KCNC3
1 1.000 0.080 19 50323182 missense variant T/C snv 2.6E-03 3.2E-03 0.700 1.000 7 2006 2015
dbSNP: rs778523009
rs778523009
KCNC3
1 1.000 0.080 19 50323026 missense variant C/T snv 2.0E-04 2.7E-04 0.700 1.000 7 2006 2015
dbSNP: rs148033381
rs148033381
KCNC3
1 1.000 0.080 19 50323524 missense variant C/T snv 2.2E-04 1.9E-04 0.700 0
dbSNP: rs1555781806
rs1555781806
KCNC3 ; LOC105372437
1 1.000 0.080 19 50329071 frameshift variant TG/- del 0.700 0
dbSNP: rs769502387
rs769502387
KCNC3
1 1.000 0.080 19 50323856 missense variant C/T snv 1.4E-05 0.700 0
dbSNP: rs879253883
rs879253883
KCNC3
1 1.000 0.080 19 50323670 missense variant G/A snv 0.700 0
dbSNP: rs958323371
rs958323371
KCNC3
1 1.000 0.080 19 50320284 missense variant C/T snv 7.5E-05 0.700 0