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: rs7756521
rs7756521
5 1.000 6 30880476 intron variant T/C snv 0.25 0.800 1.000 1 2009 2009
dbSNP: rs3131034
rs3131034
5 0.925 0.080 6 30886019 intron variant G/A snv 0.75 0.700 1.000 1 2010 2010
dbSNP: rs9295930
rs9295930
4 1.000 6 30882045 intron variant G/A snv 0.17 0.700 1.000 1 2010 2010
dbSNP: rs9468843
rs9468843
4 1.000 6 30900181 downstream gene variant T/C snv 0.17 0.700 1.000 1 2010 2010