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: rs137853859
rs137853859
3 0.882 0.120 1 23797718 missense variant G/A;T snv 7.2E-05; 8.0E-06 0.820 1.000 9 1997 2016
dbSNP: rs121908047
rs121908047
4 0.851 0.120 1 23798188 missense variant C/T snv 8.0E-06 1.4E-05 0.810 1.000 11 1997 2008
dbSNP: rs137853860
rs137853860
3 0.882 0.120 1 23796777 missense variant G/A snv 1.6E-05 7.0E-06 0.810 1.000 10 1997 2013
dbSNP: rs137853861
rs137853861
3 0.882 0.120 1 23796234 missense variant C/T snv 2.0E-05 0.810 1.000 8 1997 2006
dbSNP: rs121908045
rs121908045
1 1.000 0.120 1 23797128 missense variant A/G snv 4.1E-06 0.800 1.000 8 1997 2006
dbSNP: rs121908046
rs121908046
1 1.000 0.120 1 23798907 missense variant T/C snv 2.0E-05; 4.0E-06 7.0E-06 0.800 1.000 8 1997 2006
dbSNP: rs28940882
rs28940882
3 0.882 0.120 1 23798199 missense variant C/T snv 0.800 1.000 8 1997 2006
dbSNP: rs28940883
rs28940883
1 1.000 0.120 1 23798160 missense variant T/C snv 4.0E-06 0.800 1.000 8 1997 2006
dbSNP: rs3180383
rs3180383
3 0.882 0.120 1 23796202 missense variant G/A;T snv 0.800 1.000 8 1997 2006
dbSNP: rs28940884
rs28940884
3 0.882 0.120 1 23796722 missense variant T/C snv 1.4E-03 5.8E-03 0.710 1.000 8 1997 2006
dbSNP: rs28940885
rs28940885
2 0.925 0.120 1 23796183 missense variant C/T snv 3.5E-04 1.2E-03 0.710 1.000 8 1997 2006
dbSNP: rs1431772923
rs1431772923
1 1.000 0.120 1 23798934 missense variant G/A snv 4.0E-06 0.700 1.000 8 1997 2006
dbSNP: rs144492228
rs144492228
1 1.000 0.120 1 23798890 missense variant G/A;T snv 1.6E-05; 4.0E-06 0.700 1.000 8 1997 2006
dbSNP: rs368637540
rs368637540
3 0.882 0.120 1 23795992 missense variant C/G;T snv 1.2E-05 0.700 1.000 8 1997 2006
dbSNP: rs528467258
rs528467258
1 1.000 0.120 1 23797730 missense variant C/T snv 4.0E-06 0.700 1.000 8 1997 2006
dbSNP: rs1261697960
rs1261697960
1 1.000 0.120 1 23798645 missense variant G/T snv 4.0E-06 0.700 0