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: rs2418736
rs2418736
4 16 68120959 intron variant G/A snv 0.28 0.700 1.000 1 2009 2009
dbSNP: rs4359427
rs4359427
3 16 68168844 intron variant C/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs9932251
rs9932251
1 16 68097829 intron variant G/A snv 0.19 0.700 1.000 1 2009 2009