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: rs58030288
rs58030288
ERG
2 21 38482555 intron variant C/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs7275212
rs7275212
ERG
1 21 38480628 intron variant A/T snv 2.9E-02 0.700 1.000 1 2011 2011
dbSNP: rs78762153
rs78762153
ERG
1 21 38473352 intron variant T/C snv 1.5E-02 0.700 1.000 1 2018 2018