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: rs12407028
rs12407028
2 1 68182033 intron variant T/A;C snv 0.35 0.700 1.000 1 2012 2012
dbSNP: rs1430740
rs1430740
2 1 68191827 intron variant T/C snv 0.58 0.700 1.000 1 2014 2014