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: rs12249854
rs12249854
3 0.882 0.160 10 91426505 intron variant T/A snv 0.21 0.010 1.000 1 2011 2011
dbSNP: rs7081363
rs7081363
1 1.000 0.160 10 91410192 intron variant G/A;C snv 0.010 1.000 1 2011 2011