Variants in gene HLCS with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP
NM_001352514.2(HLCS):c.1074G>A (p.Thr358=)	rs116985497
NM_001352514.2(HLCS):c.1278G>A (p.Glu426=)	rs548505968
NM_001352514.2(HLCS):c.1331G>A (p.Arg444Gln)	rs146030669
NM_001352514.2(HLCS):c.1621-12T>C	rs367728041
NM_001352514.2(HLCS):c.1695C>T (p.Leu565=)	rs138209330
NM_001352514.2(HLCS):c.2151C>T (p.Asn717=)	rs148709879
NM_001352514.2(HLCS):c.2615G>A (p.Arg872Gln)	rs147474255
NM_001352514.2(HLCS):c.865G>A (p.Val289Ile)	rs149291867

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