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: rs200699819
rs200699819
SLC22A5
1 1.000 0.160 5 132385436 missense variant G/A snv 9.9E-05 7.0E-05 0.700 1.000 18 1999 2017