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: rs104894493
rs104894493
NR2E3
1 1.000 0.160 15 71811591 missense variant G/A snv 2.0E-04 3.1E-04 0.700 1.000 8 2000 2013