Source: CURATED ×
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: rs121908445
rs121908445
CNTNAP2
1 0.925 0.040 7 148147542 missense variant T/C snv 3.3E-04 1.7E-04 0.700 0
dbSNP: rs2710102
rs2710102
CNTNAP2
1 0.790 0.120 7 147877298 intron variant A/G;T snv 0.700 0
dbSNP: rs7794745
rs7794745
CNTNAP2
1 0.851 0.040 7 146792514 intron variant A/T snv 0.49 0.700 0