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: rs10016022
rs10016022
3 0.925 0.120 4 10445282 missense variant A/G;T snv 0.74 0.700 1.000 2 2010 2013
dbSNP: rs10016702
rs10016702
2 0.925 0.120 4 10446016 missense variant A/G;T snv 0.12; 4.0E-06 0.700 1.000 2 2010 2013
dbSNP: rs10938799
rs10938799
3 0.925 0.120 4 10441801 3 prime UTR variant G/A snv 0.21 0.700 1.000 2 2010 2013
dbSNP: rs12019277
rs12019277
3 0.925 0.120 4 10453370 non coding transcript exon variant C/A;T snv 0.700 1.000 2 2010 2013
dbSNP: rs3217
rs3217
3 0.925 0.120 4 10443026 3 prime UTR variant C/T snv 0.28 0.700 1.000 2 2010 2013
dbSNP: rs4422413
rs4422413
3 0.925 0.120 4 10441760 3 prime UTR variant T/G snv 0.28 0.700 1.000 2 2010 2013
dbSNP: rs7674156
rs7674156
3 0.925 0.120 4 10451139 non coding transcript exon variant G/C snv 0.28 0.700 1.000 2 2010 2013