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: rs1057519731
rs1057519731
2 0.925 0.040 15 66436816 missense variant G/C snv 0.720 1.000 5 2011 2014
dbSNP: rs397516792
rs397516792
6 0.827 0.280 15 66436825 missense variant C/A;G;T snv 0.720 1.000 5 2009 2015
dbSNP: rs1057519732
rs1057519732
6 0.827 0.160 15 66436824 missense variant C/A;T snv 0.700 1.000 3 2009 2012
dbSNP: rs1057519733
rs1057519733
1 1.000 0.040 15 66481793 missense variant G/A snv 0.700 1.000 3 2009 2013
dbSNP: rs1057519729
rs1057519729
6 0.827 0.080 15 66435113 missense variant A/C snv 0.700 1.000 2 2009 2013
dbSNP: rs1057519730
rs1057519730
2 1.000 0.040 15 66436786 missense variant T/A;G snv 0.700 1.000 2 2011 2012
dbSNP: rs1057519734
rs1057519734
1 1.000 0.040 15 66485086 missense variant C/T snv 0.700 1.000 2 2011 2012
dbSNP: rs1057519805
rs1057519805
3 1.000 0.040 15 66436839 missense variant T/C snv 0.700 1.000 2 2009 2013
dbSNP: rs1057519728
rs1057519728
5 0.851 0.120 15 66435103 missense variant T/A;C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs1057519735
rs1057519735
1 1.000 0.040 15 66490577 missense variant A/C snv 0.700 1.000 1 2011 2011
dbSNP: rs121908596
rs121908596
7 0.807 0.240 15 66436837 missense variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs397516790
rs397516790
2 0.925 0.200 15 66435115 missense variant A/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs727504317
rs727504317
6 0.807 0.320 15 66435145 missense variant G/A snv 0.700 1.000 1 2014 2014
dbSNP: rs869025608
rs869025608
9 0.763 0.400 15 66435117 missense variant G/C;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1057519856
rs1057519856
2 0.925 0.040 15 66436815 missense variant T/A snv 0.020 1.000 2 2014 2014