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: rs10803666
rs10803666
1 1.000 0.120 2 233930302 intron variant G/C snv 0.11 0.010 1.000 1 2017 2017
dbSNP: rs269094
rs269094
1 1.000 0.120 1 112096552 intergenic variant C/T snv 0.81 0.010 1.000 1 2017 2017