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: rs1057516168
rs1057516168
FOXL2 ; FOXL2NB
1 1.000 0.200 3 138946079 missense variant T/C snv 0.710 1.000 1 2004 2004