Variants in gene HLCS with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001352514.2(HLCS):c.1275C>T (p.Ser425=)	rs1065758	0.11920
NM_001352514.2(HLCS):c.727G>A (p.Val243Ile)	rs61732502	0.04059
NM_001352514.2(HLCS):c.567G>T (p.Glu189Asp)	rs61732504	0.03941
NM_001352514.2(HLCS):c.1969G>A (p.Gly657Arg)	rs75867009	0.00642
NM_001352514.2(HLCS):c.726C>T (p.Pro242=)	rs2230182	0.00587
NM_001352514.2(HLCS):c.1002C>T (p.Ala334=)	rs116114362	0.00352
NM_001352514.2(HLCS):c.2113G>A (p.Glu705Lys)	rs149736764	0.00315
NM_001352514.2(HLCS):c.1893-6C>T	rs139904712	0.00313
NM_001352514.2(HLCS):c.1074G>A (p.Thr358=)	rs116985497	0.00235
NM_001352514.2(HLCS):c.900G>A (p.Arg300=)	rs146019354	0.00232
NM_001352514.2(HLCS):c.1695C>T (p.Leu565=)	rs138209330	0.00087
NM_001352514.2(HLCS):c.865G>A (p.Val289Ile)	rs149291867	0.00087
NM_001352514.2(HLCS):c.2151C>T (p.Asn717=)	rs148709879	0.00012
NM_001352514.2(HLCS):c.2583C>T (p.Phe861=)	rs532108774	0.00004
NM_001352514.2(HLCS):c.1620+7del	rs140568778
NM_001352514.2(HLCS):c.1621-13_1621-10del	rs377641674

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