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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TCOF1
(E97K)
Single nucleotide variant
(missense variant)
Treacher Collins syndrome 1
+1 more
GUncertain significance
TCOF1
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
TCOF1
(A871S +1 more)
Single nucleotide variant
(missense variant)
Treacher Collins syndrome 1
+2 more
GBenign/Likely benign
LOC129994988, TCOF1
Single nucleotide variant
(intron variant)
Treacher Collins syndrome 1
GBenign/Likely benign
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