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: 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: rs2070895
rs2070895
15 0.807 0.120 15 58431740 intron variant G/A snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs1800588
rs1800588
16 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 0.800 1.000 6 2012 2019