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: rs4939921
rs4939921
1 1.000 0.040 18 49935958 intron variant T/C snv 9.4E-02 0.700 1.000 1 2008 2008