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: rs10401969
rs10401969
25 0.776 0.240 19 19296909 intron variant T/C snv 0.10 0.800 1.000 9 2010 2019
dbSNP: rs140868651
rs140868651
1 19 19321482 intron variant G/- delins 4.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs1859287
rs1859287
4 19 19311378 intron variant T/A;C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs2023883
rs2023883
4 19 19294671 intron variant G/A snv 0.19 0.700 1.000 1 2012 2012