rs111033284, MYO7A

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Multiple congenital anomalies
CUI: C0000772
Disease: Multiple congenital anomalies
350 11 77156991 missense variant G/A snv 1.6E-05 7.0E-06 0.700 1.000 13 1995 2011
Overgrowth
CUI: C1849265
Disease: Overgrowth
93 11 77156991 missense variant G/A snv 1.6E-05 7.0E-06 0.700 1.000 13 1995 2011