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: rs1049481
rs1049481
1 19 12943967 missense variant G/T snv 0.62 0.57 0.700 1.000 1 2012 2012
dbSNP: rs2974755
rs2974755
1 19 12951849 intron variant C/T snv 0.59 0.700 1.000 1 2012 2012
dbSNP: rs7395
rs7395
1 19 12953508 3 prime UTR variant G/T snv 4.2E-02 0.700 1.000 1 2012 2012