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: rs369837642
rs369837642
NT5C3A
2 7 33045761 intron variant TT/-;T;TTT delins 0.36 0.700 1.000 1 2016 2016