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: rs121908214
rs121908214
4 0.925 0.080 19 13230185 missense variant T/G snv 0.010 1.000 1 1998 1998
dbSNP: rs121908225
rs121908225
12 0.790 0.120 19 13365448 missense variant G/A snv 0.010 1.000 1 2006 2006
dbSNP: rs16022
rs16022
1 19 13298882 missense variant C/G;T snv 0.13; 4.6E-06 0.010 1.000 1 2009 2009
dbSNP: rs16023
rs16023
1 19 13298658 missense variant T/A;C snv 0.14 0.010 1.000 1 2009 2009
dbSNP: rs763054302
rs763054302
2 1.000 0.040 19 13299007 missense variant C/T snv 8.5E-05 4.9E-05 0.010 1.000 1 2014 2014
dbSNP: rs886039322
rs886039322
2 1.000 0.080 19 13312778 missense variant T/C snv 8.9E-06 7.0E-06 0.010 1.000 1 2005 2005