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: rs3753366
rs3753366
GNG12
9 0.790 0.080 1 67729450 intron variant C/G snv 0.20 0.700 1.000 1 2017 2017