FOXC2, forkhead box C2, 2303

N. diseases: 168; N. variants: 18
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs121909106
rs121909106
0.925 0.040 16 86567709 missense variant C/T snv
CUI: C1704423
Disease: Milroy Disease
Milroy Disease
Hemic and Lymphatic Diseases 0.010 1.000 1 2005 2005
dbSNP: rs121909107
rs121909107
0.925 0.040 16 86567697 missense variant G/A snv
CUI: C1704423
Disease: Milroy Disease
Milroy Disease
Hemic and Lymphatic Diseases 0.010 1.000 1 2005 2005