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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126806630, THRB
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
LOC126806630, THRB
Single nucleotide variant
(synonymous variant)
Thyroid hormone resistance, generalized, autosomal dominant
GUncertain significance
LOC126806630, THRB
(E186K +1 more)
Single nucleotide variant
(missense variant)
Thyroid hormone resistance, generalized, autosomal dominant
GUncertain significance
LOC126806630, THRB
Single nucleotide variant
(synonymous variant)
Thyroid hormone resistance syndrome
GUncertain significance
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