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: rs17085106
rs17085106
1 1.000 0.080 18 71771837 intron variant G/T snv 6.3E-02 0.800 1.000 1 2009 2009