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: rs849563
rs849563
1 1.000 0.040 2 205745778 synonymous variant T/A;G snv 4.0E-06; 0.19 0.020 1.000 2 2007 2017
dbSNP: rs849578
rs849578
1 1.000 0.040 2 205738798 intron variant G/A;T snv 0.010 1.000 1 2007 2007