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: rs104894158
rs104894158
5 0.851 0.080 10 62813835 missense variant A/T snv 0.010 1.000 1 2009 2009
dbSNP: rs104894159
rs104894159
5 0.827 0.080 10 62813413 missense variant G/A snv 0.010 1.000 1 2005 2005
dbSNP: rs104894161
rs104894161
6 0.807 0.080 10 62813563 missense variant G/A snv 0.010 1.000 1 2005 2005
dbSNP: rs281865137
rs281865137
4 0.851 0.080 10 62813496 missense variant C/T snv 0.010 1.000 1 2000 2000
dbSNP: rs281865139
rs281865139
2 0.925 0.080 10 62813478 missense variant G/T snv 0.010 1.000 1 2012 2012
dbSNP: rs372491511
rs372491511
1 1.000 0.080 10 62814078 missense variant G/A;T snv 8.0E-06 1.4E-05 0.010 1.000 1 2005 2005