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: rs61867293
rs61867293
2 1.000 0.040 10 104804166 intron variant C/T snv 0.15 0.700 1.000 1 2019 2019