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: rs13030973
rs13030973
4 0.925 0.120 2 27705930 non coding transcript exon variant T/C snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs4616435
rs4616435
4 0.925 0.120 2 27710775 intron variant C/T snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs6727215
rs6727215
4 0.925 0.120 2 27711864 intron variant G/A snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs6727388
rs6727388
4 0.925 0.120 2 27709720 intron variant A/G;T snv 0.700 1.000 1 2010 2010