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: rs10503929
rs10503929
NRG1
3 0.925 0.040 8 32756465 missense variant T/C snv 0.13 0.13 0.030 1.000 3 2011 2018