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: rs3736228
rs3736228
13 0.752 0.400 11 68433827 missense variant C/T snv 0.13 0.11 0.090 1.000 9 2005 2017
dbSNP: rs4988321
rs4988321
4 0.851 0.160 11 68406721 missense variant G/A;C snv 3.8E-02 0.040 0.750 4 2005 2019
dbSNP: rs1784235
rs1784235
1 1.000 0.080 11 68418032 intron variant C/T snv 0.69 0.010 1.000 1 2007 2007
dbSNP: rs312009
rs312009
2 0.925 0.080 11 68309770 upstream gene variant T/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs491347
rs491347
2 0.925 0.200 11 68402220 intron variant G/A;T snv 0.010 1.000 1 2007 2007
dbSNP: rs545382
rs545382
1 1.000 0.080 11 68403545 synonymous variant T/C snv 0.91 0.83 0.010 1.000 1 2010 2010
dbSNP: rs61889560
rs61889560
1 1.000 0.080 11 68423568 missense variant G/A;T snv 2.5E-03 0.010 1.000 1 2005 2005
dbSNP: rs627174
rs627174
1 1.000 0.080 11 68396046 intron variant C/T snv 0.74 0.010 1.000 1 2013 2013
dbSNP: rs901824
rs901824
1 1.000 0.080 11 68438705 intron variant T/C snv 7.5E-02 1.0E-01 0.010 1.000 1 2013 2013