"Fulgent Genetics, Fulgent Genetics"[submitter] AND "HTT"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809691	NM_001388492.1(HTT):c.99_100del (p.Gln34fs)	HTT, LOC109461479 +1 more (Q34fs)	Deletion (frameshift variant)	Huntington disease +1 more	GLikely benign
Select item 1671702	NM_001388492.1(HTT):c.4638C>G (p.Val1546=)	HTT	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1599166	NM_001388492.1(HTT):c.7765+10G>A	HTT	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign

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