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: rs11865121
rs11865121
1 1.000 0.080 16 11072831 intron variant C/A snv 0.40 0.800 1.000 1 2009 2009
dbSNP: rs7200786
rs7200786
2 0.882 0.200 16 11083944 intron variant A/G snv 0.59 0.800 1.000 1 2011 2011
dbSNP: rs12927355
rs12927355
2 0.882 0.240 16 11100914 intron variant C/A;T snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs6498160
rs6498160
1 1.000 0.080 16 11105590 intron variant T/C snv 0.51 0.700 1.000 1 2017 2017
dbSNP: rs6498168
rs6498168
1 1.000 0.080 16 11141273 intron variant T/G snv 0.71 0.700 1.000 1 2016 2016