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: rs121917724
rs121917724
1 1.000 0.040 19 33387892 missense variant C/T snv 1.8E-05 3.5E-05 0.800 1.000 7 1990 2017
dbSNP: rs121917721
rs121917721
1 1.000 0.040 19 33401862 missense variant C/G;T snv 2.4E-05; 3.2E-05 0.800 1.000 4 1990 2002
dbSNP: rs121917722
rs121917722
1 1.000 0.040 19 33464060 missense variant C/T snv 2.4E-05 0.800 1.000 4 1990 2002
dbSNP: rs121917723
rs121917723
1 1.000 0.040 19 33401855 missense variant C/T snv 4.4E-05 2.1E-05 0.800 1.000 4 1990 2002
dbSNP: rs745834191
rs745834191
1 1.000 0.040 19 33413621 inframe deletion TAG/- delins 1.6E-04 1.3E-04 0.700 1.000 2 2004 2013
dbSNP: rs747700126
rs747700126
1 1.000 0.040 19 33463032 missense variant C/A;G;T snv 1.2E-05 0.700 1.000 1 2010 2010
dbSNP: rs797045185
rs797045185
1 1.000 0.040 19 33391344 missense variant A/C;G snv 4.1E-06 0.700 1.000 1 2010 2010
dbSNP: rs121917725
rs121917725
1 1.000 0.040 19 33411697 stop gained G/A;C snv 1.2E-05; 4.0E-06 0.700 0
dbSNP: rs267606943
rs267606943
1 1.000 0.040 19 33464006 missense variant G/A snv 0.700 0
dbSNP: rs267606944
rs267606944
1 1.000 0.040 19 33388000 missense variant C/T snv 0.700 0
dbSNP: rs757386104
rs757386104
1 1.000 0.040 19 33387465 inframe deletion CTC/- delins 1.4E-05 0.700 0
dbSNP: rs794728008
rs794728008
1 1.000 0.040 19 33463987 stop gained -/TCACGGTGGGCCT delins 0.700 0