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: rs7250897
rs7250897
2 0.882 0.080 19 40277326 intron variant T/A;C snv 0.010 1.000 1 2017 2017
dbSNP: rs7254617
rs7254617
5 0.882 0.120 19 40285605 upstream gene variant G/A;C;T snv 0.010 1.000 1 2012 2012