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: rs3790567
rs3790567
1 0.851 0.240 1 67356694 intron variant A/G snv 0.61 0.800 1.000 2 2009 2010
dbSNP: rs72678531
rs72678531
1 1.000 0.080 1 67332762 intron variant T/C snv 0.17 0.800 1.000 2 2012 2012
dbSNP: rs10889681
rs10889681
1 0.925 0.160 1 67333487 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs11209050
rs11209050
1 1.000 0.080 1 67326053 intron variant A/C snv 0.68 0.700 1.000 1 2011 2011
dbSNP: rs11209051
rs11209051
1 1.000 0.080 1 67333212 intron variant C/T snv 0.73 0.700 1.000 1 2012 2012
dbSNP: rs56194793
rs56194793
1 1.000 0.080 1 67324915 intron variant T/C snv 0.700 1.000 1 2012 2012
dbSNP: rs6659932
rs6659932
1 0.827 0.240 1 67336688 intron variant A/C snv 0.81 0.700 1.000 1 2012 2012