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: rs365132
rs365132
2 5 176951573 synonymous variant G/T snv 0.51 0.58 0.800 1.000 3 2009 2015
dbSNP: rs58279426
rs58279426
1 5 177021138 intron variant T/C snv 0.57 0.700 1.000 1 2019 2019