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: rs10506328
rs10506328
1 12 54293448 intron variant A/C snv 0.75 0.800 1.000 2 2009 2014
dbSNP: rs35979828
rs35979828
9 12 54292096 intron variant C/T snv 5.0E-02 0.700 1.000 1 2016 2016