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: rs1800561
rs1800561
7 0.807 0.240 4 15824935 missense variant C/A;T snv 8.0E-06; 4.4E-04 0.010 1.000 1 2009 2009
dbSNP: rs6449182
rs6449182
6 0.807 0.160 4 15778830 intron variant C/G snv 0.22 0.010 1.000 1 2009 2009