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: rs28927680
rs28927680
4 11 116748357 3 prime UTR variant C/G;T snv 0.800 1.000 5 2008 2019
dbSNP: rs10790162
rs10790162
7 0.882 0.160 11 116768388 intron variant A/G;T snv 0.93 0.800 1.000 3 2011 2019
dbSNP: rs11825181
rs11825181
2 11 116755542 intron variant G/A snv 0.10 0.800 1.000 1 2011 2011
dbSNP: rs180327
rs180327
5 11 116752943 intron variant C/T snv 0.58 0.700 1.000 2 2012 2012
dbSNP: rs6589565
rs6589565
5 11 116769521 intron variant A/G snv 0.93 0.700 1.000 2 2012 2012
dbSNP: rs11820589
rs11820589
5 1.000 0.040 11 116763146 missense variant G/A snv 7.8E-02 0.10 0.700 1.000 1 2012 2012
dbSNP: rs12292921
rs12292921
1 11 116751247 intron variant T/G snv 0.10 0.700 1.000 1 2009 2009
dbSNP: rs180326
rs180326
1 11 116753987 intron variant G/T snv 0.57 0.700 1.000 1 2017 2017
dbSNP: rs2075295
rs2075295
1 11 116757685 intron variant T/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs3741300
rs3741300
1 11 116760974 intron variant G/A snv 0.36 0.34 0.700 1.000 1 2012 2012
dbSNP: rs4938310
rs4938310
1 11 116759233 intron variant C/T snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs79624460
rs79624460
1 11 116764566 intron variant C/T snv 2.7E-02 0.700 1.000 1 2019 2019