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: rs286262
rs286262
1 1.000 0.080 19 11736800 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs4804636
rs4804636
1 1.000 0.080 19 11731508 intron variant C/T snv 0.29 0.700 1.000 1 2013 2013