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: rs324650
rs324650
CHRM2 ; LOC349160
5 0.827 0.080 7 137008914 intron variant T/A snv 0.55 0.010 1.000 1 2004 2004