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
2 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 1 2012 2012
dbSNP: rs17129789
rs17129789
2 0.925 0.080 1 67324915 intron variant T/C snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs6679356
rs6679356
1 0.925 0.200 1 67354511 intron variant C/T snv 0.75 0.700 1.000 1 2015 2015