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: rs11889798
rs11889798
2 1.000 0.120 2 227616703 intron variant C/T snv 0.13 0.010 1.000 1 2019 2019