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: rs1552272
rs1552272
1 16 85419089 intron variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs4783189
rs4783189
1 16 85383406 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs4843185
rs4843185
1 16 85656732 intron variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs76563408
rs76563408
1 16 85380749 intron variant G/A snv 6.0E-02 0.700 1.000 1 2016 2016