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: rs2229707
rs2229707
2 0.925 0.080 11 74006202 missense variant C/T snv 1.0E-02 3.9E-02 0.700 0
dbSNP: rs150016118
rs150016118
6 0.882 0.120 11 74006339 missense variant A/G snv 1.7E-05 6.3E-05 0.030 0.333 3 2007 2014
dbSNP: rs777659543
rs777659543
6 0.882 0.120 11 74006231 missense variant G/A snv 4.0E-06 0.030 0.333 3 2007 2014
dbSNP: rs1800849
rs1800849
5 0.851 0.160 11 74009120 upstream gene variant G/A;T snv 0.020 1.000 2 2007 2017
dbSNP: rs1626521
rs1626521
1 1.000 0.080 11 74003294 intron variant G/A snv 0.32 0.010 1.000 1 2015 2015
dbSNP: rs1726745
rs1726745
1 1.000 0.080 11 74002397 intron variant T/C snv 0.57 0.010 1.000 1 2009 2009
dbSNP: rs373468564
rs373468564
1 1.000 0.080 11 74004553 missense variant C/T snv 3.2E-05 6.3E-05 0.010 1.000 1 2012 2012
dbSNP: rs74907838
rs74907838
1 1.000 0.080 11 74006174 missense variant G/A snv 8.9E-04 3.6E-03 0.010 1.000 1 2012 2012
dbSNP: rs765633988
rs765633988
1 1.000 0.080 11 74003897 stop gained G/A snv 4.0E-06 2.8E-05 0.010 1.000 1 2012 2012