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: rs4460079
rs4460079
2 4 113940144 intron variant C/T snv 0.58 0.700 1.000 1 2013 2013
dbSNP: rs7658266
rs7658266
2 4 113942550 intron variant T/A;C snv 0.700 1.000 1 2013 2013