Details for Combination OLI1082

VARIANTS NKX2-1:p.Gly352Ser in Heterozygous form; TG:c.4859C>T, p.Thr1620Met in Heterozygous form
GENE COMBINATION NKX2-1; TG
OLIGOGENIC EFFECT Unknown
ETHNICITY East Asian
OMIM IDS N.A.
DISEASES Congenital hypothyroidism
REFERENCES 34374102
SCORES
FAMmanual
2

STAT
manualknowledgemeta
101

GENE
manualmanual harmonizedknowledgemeta
0000

VAR
manualknowledgemeta
000

FUN
manualmeta
00

FINAL
manualmeta
00


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