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: rs9551963
rs9551963
6 0.851 0.160 13 30758410 intron variant A/C;T snv 0.020 1.000 2 2012 2014
dbSNP: rs10507391
rs10507391
10 0.776 0.320 13 30737959 intron variant A/T snv 0.52 0.010 < 0.001 1 2015 2015
dbSNP: rs4073259
rs4073259
4 0.882 0.160 13 30732134 intron variant G/A snv 0.49 0.010 1.000 1 2012 2012
dbSNP: rs4147064
rs4147064
2 1.000 0.120 13 30745981 intron variant T/C snv 0.50 0.010 1.000 1 2012 2012
dbSNP: rs4769055
rs4769055
1 1.000 0.120 13 30735693 intron variant C/A snv 0.41 0.47 0.010 1.000 1 2008 2008
dbSNP: rs9579646
rs9579646
6 0.851 0.160 13 30736442 intron variant G/A;T snv 0.010 1.000 1 2012 2012