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: rs10008637
rs10008637
2 4 76492991 intron variant T/A;C snv 0.35 0.700 1.000 1 2016 2016
dbSNP: rs2870238
rs2870238
2 4 76451926 intron variant C/T snv 0.39 0.700 1.000 1 2016 2016