List of variants in gene HLCS reported as uncertain significance for not specified

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001352514.2(HLCS):c.865G>A (p.Val289Ile)	rs149291867	0.00087
NM_001352514.2(HLCS):c.2341G>A (p.Asp781Asn)	rs149399432	0.00004
NM_001352514.2(HLCS):c.2519G>C (p.Gly840Ala)	rs764148793	0.00001
NM_001352514.2(HLCS):c.2585A>C (p.Asp862Ala)	rs752737867	0.00001
NM_001352514.2(HLCS):c.442A>G (p.Met148Val)	rs764841449	0.00001
NM_001352514.2(HLCS):c.2151C>G (p.Asn717Lys)
NM_001352514.2(HLCS):c.2268_2270del (p.Thr757del)	rs1555882090
NM_001352514.2(HLCS):c.2450+4A>G
NM_001352514.2(HLCS):c.2600del (p.Leu867fs)	rs761447836

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