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: rs2104286
rs2104286
25 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.900 1.000 14 2007 2019
dbSNP: rs12722489
rs12722489
3 0.882 0.160 10 6060049 intron variant C/T snv 0.11 0.850 1.000 7 2007 2018
dbSNP: rs3118470
rs3118470
10 0.752 0.360 10 6059750 intron variant T/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs1107345
rs1107345
2 0.925 0.160 10 6045332 intron variant G/T snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs12253981
rs12253981
1 1.000 0.080 10 6050383 intron variant T/G snv 0.29 0.700 1.000 1 2017 2017
dbSNP: rs12722561
rs12722561
1 1.000 0.080 10 6027930 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs706778
rs706778
19 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.700 1.000 1 2011 2011
dbSNP: rs1191996028
rs1191996028
1 1.000 0.080 10 6025978 missense variant C/T snv 4.0E-06 0.010 1.000 1 2011 2011
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: rs1570538
rs1570538
1 1.000 0.080 10 6011605 3 prime UTR variant C/T snv 0.42 0.010 1.000 1 2009 2009
dbSNP: rs791589
rs791589
1 1.000 0.080 10 6047608 intron variant G/A snv 0.71 0.010 1.000 1 2009 2009