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: rs121908480
rs121908480
SLC7A9
1 1.000 0.120 19 32864261 missense variant C/T snv 2.7E-04 1.7E-04 0.800 1.000 14 1999 2015