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: rs11643718
rs11643718
10 0.807 0.240 16 56899607 missense variant G/A snv 0.11 8.4E-02 0.020 1.000 2 2008 2018
dbSNP: rs2399594
rs2399594
1 16 56912285 intron variant A/G snv 0.39 0.010 1.000 1 2015 2015
dbSNP: rs5804
rs5804
1 16 56894607 synonymous variant C/T snv 0.13 9.3E-02 0.010 1.000 1 2014 2014
dbSNP: rs6499857
rs6499857
1 16 56901178 intron variant G/C snv 0.31 0.010 1.000 1 2014 2014
dbSNP: rs711746
rs711746
1 16 56912892 intron variant T/C;G snv 0.010 1.000 1 2015 2015
dbSNP: rs7187932
rs7187932
1 16 56897792 intron variant G/A snv 0.25 0.010 1.000 1 2015 2015
dbSNP: rs8063291
rs8063291
1 16 56896339 intron variant T/C snv 0.21 0.010 1.000 1 2014 2014