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: rs121908864
rs121908864
6 0.851 0.120 14 81143416 missense variant T/C;G snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs28937584
rs28937584
4 0.925 0.080 14 81143955 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs750198847
rs750198847
1 14 81143650 missense variant G/A snv 3.6E-05 4.2E-05 0.010 1.000 1 2005 2005
dbSNP: rs764330550
rs764330550
1 14 81143730 missense variant G/T snv 4.0E-06 0.010 1.000 1 2005 2005