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: rs11672660
rs11672660
5 19 45676926 intron variant C/T snv 0.18 0.17 0.700 1.000 1 2015 2015
dbSNP: rs2238691
rs2238691
3 19 45675785 intron variant G/A snv 0.17 0.700 1.000 1 2019 2019