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: rs1799983
rs1799983
NOS3
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2014 2014
dbSNP: rs3832043
rs3832043
UGT1A10 ; UGT1A8 ; UGT1A9
1 1.000 0.040 2 233671808 intron variant TT/-;T;TTT delins 0.59 0.010 1.000 1 2016 2016