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: rs5030359
rs5030359
3 19 10277786 intron variant G/A snv 2.1E-03 0.700 1.000 2 2012 2012
dbSNP: rs5030339
rs5030339
5 19 10269461 intron variant G/A snv 3.4E-03 0.700 1.000 1 2012 2012
dbSNP: rs5030361
rs5030361
4 19 10278833 intron variant C/T snv 6.8E-04 0.700 1.000 1 2012 2012