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: rs1421589
rs1421589
NRXN1
1 1.000 0.080 2 50063015 intron variant A/G;T snv 0.010 1.000 1 2018 2018