List of variants in gene HLCS reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001352514.2(HLCS):c.1550C>T (p.Thr517Ile)	rs575286749	0.00013
NM_001352514.2(HLCS):c.2407C>T (p.Pro803Ser)	rs538159086	0.00013
NM_001352514.2(HLCS):c.2584G>A (p.Asp862Asn)	rs140014588	0.00003
NM_001352514.2(HLCS):c.1856C>G (p.Ala619Gly)	rs767190021
NM_001352514.2(HLCS):c.2600del (p.Leu867fs)	rs761447836

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