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: rs1824024
rs1824024
CHRM2 ; LOC349160
4 0.851 0.160 7 136958947 intron variant C/A snv 0.65 0.010 1.000 1 2005 2005