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: rs165501
rs165501
1 1.000 0.040 3 10167559 intron variant T/A;C snv 0.010 1.000 1 2019 2019