Source: ALL
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: rs150794546
rs150794546
BRD2
1 1.000 0.040 6 32976655 missense variant G/A snv 4.1E-06 7.0E-06 0.010 < 0.001 1 2008 2008