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: rs964184
rs964184
47 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.800 1.000 6 2010 2019
dbSNP: rs6589566
rs6589566
10 0.882 0.080 11 116781707 intron variant G/A;C;T snv 0.800 1.000 1 2008 2008
dbSNP: rs113932726
rs113932726
1 11 116779922 intron variant C/T snv 9.8E-03 0.700 1.000 1 2018 2018
dbSNP: rs2075290
rs2075290
10 0.882 0.160 11 116782580 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2266788
rs2266788
19 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 0.700 1.000 1 2018 2018