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: rs7311607
rs7311607
1 12 2413815 intron variant A/G snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs7312105
rs7312105
2 12 2414189 intron variant A/G snv 0.34 0.700 1.000 1 2012 2012