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: rs121913627
rs121913627
8 0.851 0.080 14 23427657 missense variant C/A;G;T snv 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs121913647
rs121913647
4 0.925 0.160 14 23417173 missense variant C/A;G;T snv 1.6E-05 0.010 1.000 1 2010 2010
dbSNP: rs121913653
rs121913653
3 0.925 0.160 14 23429040 missense variant G/A snv 2.3E-04 7.0E-05 0.010 1.000 1 2020 2020
dbSNP: rs45544633
rs45544633
4 1.000 0.080 14 23417174 missense variant G/A snv 0.010 1.000 1 2010 2010