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: rs4805885
rs4805885
1 19 33415217 intron variant T/C snv 0.59 0.800 1.000 1 2012 2012
dbSNP: rs731839
rs731839
5 19 33408159 intron variant G/A snv 0.63 0.800 1.000 1 2012 2012
dbSNP: rs889140
rs889140
1 19 33398094 intron variant G/A;C snv 0.800 1.000 1 2014 2014