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: rs224278
rs224278
1 1.000 0.040 10 62820815 intron variant C/T snv 0.39 0.800 1.000 1 2012 2012
dbSNP: rs944684
rs944684
1 1.000 0.040 10 62916616 intron variant C/T snv 0.80 0.700 1.000 1 2012 2012