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: rs200406921
rs200406921
SLC5A1
1 1.000 0.120 22 32099305 missense variant C/A;T snv 2.0E-05; 4.0E-06 0.710 1.000 1 1999 1999