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: rs760264924
rs760264924
SLC7A9
1 1.000 0.120 19 32842191 missense variant T/C snv 1.2E-05 7.0E-06 0.700 1.000 10 1999 2010