Details for Combination OLI580

VARIANTS NKX2-1:p.Arg151Cys in Heterozygous form; TG:p.Asp1767Gly in Heterozygous form
GENE COMBINATION NKX2-1; TG
OLIGOGENIC EFFECT Unknown
ETHNICITY European/Caucasian
OMIM IDS N.A.
DISEASES Congenital hypothyroidism
REFERENCES 28444304
SCORES
FAMmanual
0

STAT
manualknowledgemeta
000

GENE
manualmanual harmonizedknowledgemeta
0000

VAR
manualknowledgemeta
000

FUN
manualmeta
00

FINAL
manualmeta
00


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