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: rs1420101
rs1420101
8 0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 0.710 0.500 2 2010 2019
dbSNP: rs6543124
rs6543124
1 1.000 0.120 2 102370999 intron variant T/A snv 0.44 0.700 1.000 1 2019 2019