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
62 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 0.820 1.000 2 2005 2016
dbSNP: rs141178472
rs141178472
2 0.925 0.080 3 179234393 3 prime UTR variant T/C snv 3.0E-03 3.3E-03 0.010 1.000 1 2015 2015
dbSNP: rs2699887
rs2699887
11 0.763 0.280 3 179148620 intron variant C/T snv 0.18 0.010 < 0.001 1 2015 2015