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: rs73110464
rs73110464
17 0.708 0.280 12 52918828 intron variant C/T snv 0.12 0.700 1.000 1 2016 2016
dbSNP: rs4919743
rs4919743
5 0.925 0.080 12 52915800 intron variant G/A snv 0.13 0.010 1.000 1 2011 2011
dbSNP: rs55958994
rs55958994
3 0.925 0.080 12 52907235 intron variant C/T snv 0.12 0.010 1.000 1 2019 2019