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: rs587776998
rs587776998
KCTD1
1 1.000 0.200 18 26501147 missense variant G/A;T snv 4.0E-06 0.800 1.000 1 2013 2013
dbSNP: rs587776999
rs587776999
KCTD1
1 1.000 0.200 18 26501144 missense variant G/A;C;T snv 0.800 1.000 1 2013 2013
dbSNP: rs587777000
rs587777000
KCTD1
1 1.000 0.200 18 26501137 missense variant G/A;T snv 4.0E-06 0.800 1.000 1 2013 2013
dbSNP: rs587777001
rs587777001
KCTD1
1 1.000 0.200 18 26501138 missense variant T/G snv 0.800 1.000 1 2013 2013
dbSNP: rs587777002
rs587777002
KCTD1
1 1.000 0.200 18 26476603 missense variant T/G snv 0.800 1.000 1 2013 2013
dbSNP: rs587777003
rs587777003
KCTD1
1 1.000 0.200 18 26476639 missense variant C/T snv 0.800 1.000 1 2013 2013
dbSNP: rs878853124
rs878853124
KCTD1
1 1.000 0.200 18 26476617 missense variant G/T snv 0.700 1.000 1 2013 2013
dbSNP: rs878853125
rs878853125
KCTD1
1 1.000 0.200 18 26501178 missense variant G/A snv 0.700 1.000 1 2013 2013