"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC126862720"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 789236	NM_001942.4(DSG1):c.2216T>C (p.Ile739Thr)	DSG1, DSG1-AS1 +1 more (I739T)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +2 more	GBenign/Likely benign
Select item 781729	NM_001942.4(DSG1):c.2622C>T (p.Gly874=)	DSG1, DSG1-AS1 +1 more	Single nucleotide variant (synonymous variant)	Palmoplantar keratoderma i, striate, focal, or diffuse +2 more	GBenign/Likely benign