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: rs17116384
rs17116384
3 11 114110519 intron variant A/G snv 0.25 0.700 1.000 1 2016 2016
dbSNP: rs73000929
rs73000929
2 11 114082900 intron variant G/A;T snv 2.1E-02 0.700 1.000 1 2016 2016