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: rs564799
rs564799
2 0.925 0.160 3 160011200 intron variant C/T snv 0.33 0.700 1.000 2 2015 2016
dbSNP: rs564976
rs564976
1 1.000 0.080 3 160011272 intron variant G/A snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs77583790
rs77583790
3 0.882 0.080 3 159976265 intron variant G/A;C snv 0.700 1.000 1 2015 2015