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: rs764059
rs764059
NRG1
1 1.000 0.040 8 32673773 intron variant G/A snv 0.80 0.010 < 0.001 1 2013 2013