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: rs121913279
rs121913279
101 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 0.090 1.000 9 2012 2018
dbSNP: rs104886003
rs104886003
71 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 0.030 1.000 3 2013 2016
dbSNP: rs121913274
rs121913274
33 0.645 0.320 3 179218304 missense variant A/C;G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs2699887
rs2699887
11 0.763 0.280 3 179148620 intron variant C/T snv 0.18 0.010 1.000 1 2017 2017
dbSNP: rs778184105
rs778184105
2 3 179199098 missense variant C/A snv 4.1E-06 0.010 1.000 1 2010 2010