rs1554616628, YWHAG

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.
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 56
4 1.000 7 76329927 missense variant G/A snv 0.800 1.000 1 2017 2017
Encephalopathies
CUI: C0085584
Disease: Encephalopathies
64 1.000 7 76329927 missense variant G/A snv 0.010 1.000 1 2017 2017