Gene: CNTNAP2 ×
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: rs1718101
rs1718101
CNTNAP2
1 1.000 0.040 7 146425696 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs7794745
rs7794745
CNTNAP2
6 0.851 0.040 7 146792514 intron variant A/T snv 0.49 0.040 0.750 4 2011 2017
dbSNP: rs2710102
rs2710102
CNTNAP2
12 0.790 0.120 7 147877298 intron variant A/G;T snv 0.020 0.500 2 2011 2013
dbSNP: rs10500171
rs10500171
CNTNAP2
1 1.000 0.040 7 147183313 intron variant A/G snv 0.52 0.010 1.000 1 2010 2010
dbSNP: rs2253031
rs2253031
CNTNAP2
1 1.000 0.040 7 147934809 intron variant A/C;G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs2710093
rs2710093
CNTNAP2
1 1.000 0.040 7 147935043 intron variant G/C snv 0.69 0.010 1.000 1 2013 2013