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: rs11573260
rs11573260
1 1 20083047 intron variant C/T snv 8.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs818678
rs818678
1 1 20039837 intron variant T/C;G snv 0.700 1.000 1 2019 2019