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: rs2710102
rs2710102
CNTNAP2
12 0.790 0.120 7 147877298 intron variant A/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs6944808
rs6944808
CNTNAP2
2 7 147555456 intron variant G/A snv 0.70 0.010 1.000 1 2011 2011