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: rs3181077
rs3181077
2 1.000 0.080 3 46209161 intron variant C/T snv 0.80 0.010 1.000 1 2015 2015