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: rs1801239
rs1801239
1 0.827 0.160 10 16877053 missense variant T/C;G snv 8.9E-02; 8.0E-06 0.800 1.000 2 2011 2019