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: rs2242446
rs2242446
SLC6A2
9 0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 0.010 1.000 1 2005 2005
dbSNP: rs2397771
rs2397771
SLC6A2
2 0.925 0.080 16 55655175 upstream gene variant C/A;G;T snv 0.010 1.000 1 2005 2005