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: rs10504473
rs10504473
NCOA2
1 1.000 0.080 8 70348097 intron variant A/C snv 0.24 0.010 1.000 1 2015 2015