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: rs121909326
rs121909326
3 0.882 0.160 19 13235219 missense variant A/G snv 0.700 0
dbSNP: rs1555767914
rs1555767914
1 1.000 0.080 19 13335828 missense variant G/A snv 0.700 0
dbSNP: rs794727411
rs794727411
5 0.851 0.160 19 13261526 missense variant C/G;T snv 0.700 0
dbSNP: rs886037945
rs886037945
6 0.827 0.160 19 13303584 missense variant C/T snv 0.700 0
dbSNP: rs746795369
rs746795369
6 0.827 0.080 1 160139969 missense variant C/A;T snv 1.2E-05; 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs121918616
rs121918616
3 0.882 0.080 1 160130283 missense variant G/A snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs121908217
rs121908217
9 0.851 0.120 19 13308452 missense variant C/T snv 4.0E-06 0.800 1.000 10 1996 2017
dbSNP: rs759252101
rs759252101
1 1.000 0.080 19 13212143 missense variant C/G snv 4.0E-06 0.010 < 0.001 1 2012 2012
dbSNP: rs886039322
rs886039322
2 1.000 0.080 19 13312778 missense variant T/C snv 8.9E-06 7.0E-06 0.010 < 0.001 1 2005 2005
dbSNP: rs768048563
rs768048563
2 0.925 0.120 19 13298829 missense variant C/T snv 2.6E-05 0.010 1.000 1 2003 2003
dbSNP: rs121918799
rs121918799
14 0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 0.010 1.000 1 2013 2013
dbSNP: rs41276886
rs41276886
2 0.925 0.080 19 13317310 missense variant C/T snv 4.5E-03 4.4E-03 0.010 1.000 1 2010 2010