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: rs4775041
rs4775041
8 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.800 1.000 3 2008 2018
dbSNP: rs10468017
rs10468017
12 0.851 0.120 15 58386313 intron variant C/T snv 0.24 0.800 1.000 2 2009 2018
dbSNP: rs261332
rs261332
20 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 0.800 1.000 2 2012 2016
dbSNP: rs588136
rs588136
5 15 58438299 intron variant C/G;T snv 0.800 1.000 2 2012 2017