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: rs1004072779
rs1004072779
ERG
2 0.925 0.080 21 38403547 missense variant T/C snv 2.1E-05 0.010 1.000 1 2009 2009
dbSNP: rs746001963
rs746001963
ERG
3 0.925 0.080 21 38383659 missense variant A/T snv 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs919467999
rs919467999
ERG
2 0.925 0.080 21 38383632 missense variant G/A snv 0.010 1.000 1 2020 2020