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: rs6265
rs6265
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.100 0.869 84 2003 2019
dbSNP: rs759834365
rs759834365
237 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 0.100 0.872 78 2003 2019
dbSNP: rs746682028
rs746682028
36 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.040 0.750 4 2007 2018
dbSNP: rs10835210
rs10835210
4 0.882 0.040 11 27674363 intron variant C/A;G snv 0.020 1.000 2 2016 2016
dbSNP: rs7103411
rs7103411
15 0.752 0.160 11 27678578 intron variant C/T snv 0.82 0.020 1.000 2 2015 2015
dbSNP: rs11030101
rs11030101
10 0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 0.010 1.000 1 2012 2012
dbSNP: rs11030104
rs11030104
12 0.790 0.240 11 27662970 intron variant A/G snv 0.16 0.010 1.000 1 2015 2015
dbSNP: rs1402139464
rs1402139464
3 0.882 0.160 11 27701009 5 prime UTR variant G/A;T snv 8.4E-06 0.010 1.000 1 2009 2009
dbSNP: rs2030324
rs2030324
6 0.827 0.120 11 27705368 intron variant A/G snv 0.49 0.010 1.000 1 2016 2016
dbSNP: rs56164415
rs56164415
6 0.851 0.120 11 27700188 5 prime UTR variant G/A snv 5.9E-02 0.010 1.000 1 2013 2013
dbSNP: rs893924483
rs893924483
23 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 0.010 < 0.001 1 2005 2005
dbSNP: rs988748
rs988748
3 0.882 0.120 11 27703198 intron variant C/G snv 0.83 0.010 1.000 1 2006 2006