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: rs7818511
rs7818511
GSR
1 1.000 8 30719572 intron variant T/C snv 0.76 0.010 1.000 1 2018 2018