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: rs61839660
rs61839660
9 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 0.800 1.000 2 2012 2015
dbSNP: rs706778
rs706778
19 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.750 1.000 6 2007 2015
dbSNP: rs12722495
rs12722495
5 0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 0.710 1.000 2 2011 2019
dbSNP: rs3118470
rs3118470
10 0.752 0.360 10 6059750 intron variant T/A;C snv 0.070 1.000 7 2007 2017
dbSNP: rs2104286
rs2104286
25 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.060 0.833 6 2009 2019
dbSNP: rs12722496
rs12722496
2 0.925 0.160 10 6054704 intron variant A/G snv 7.5E-02 0.010 1.000 1 2015 2015
dbSNP: rs7093069
rs7093069
1 1.000 0.120 10 6021356 intron variant C/T snv 0.18 0.010 1.000 1 2012 2012