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: rs1881492
rs1881492
CHRNG
2 1.000 2 232542288 intron variant T/C;G snv 0.700 1.000 1 2013 2013