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: rs121908869
rs121908869
5 0.882 0.160 14 80955802 missense variant G/C snv 4.0E-05 7.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs1294870139
rs1294870139
2 0.925 0.120 14 81143638 missense variant T/C snv 8.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs139892516
rs139892516
2 0.925 0.120 14 81143649 missense variant C/G;T snv 4.0E-06; 2.8E-05 0.010 1.000 1 2009 2009
dbSNP: rs189261858
rs189261858
8 0.776 0.160 14 81143407 missense variant G/A;T snv 2.3E-04 0.010 1.000 1 2010 2010