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: rs110402
rs110402
12 0.790 0.120 17 45802681 intron variant G/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs173365
rs173365
3 0.882 0.080 17 45823708 intron variant A/G snv 0.55 0.010 1.000 1 2013 2013
dbSNP: rs17689966
rs17689966
1 1.000 0.080 17 45833089 intron variant G/A snv 0.63 0.56 0.010 1.000 1 2013 2013