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

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001352514.2(HLCS):c.1074G>A (p.Thr358=)	rs116985497	0.00235
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.1331G>A (p.Arg444Gln)	rs146030669	0.00074
NM_001352514.2(HLCS):c.1621-12T>C	rs367728041	0.00032
NM_001352514.2(HLCS):c.2615G>A (p.Arg872Gln)	rs147474255	0.00018
NM_001352514.2(HLCS):c.2151C>T (p.Asn717=)	rs148709879	0.00012
NM_001352514.2(HLCS):c.1278G>A (p.Glu426=)	rs548505968	0.00006
NM_001352514.2(HLCS):c.569C>T (p.Pro190Leu)	rs534858065	0.00003
NM_001352514.2(HLCS):c.494-25TC[4]	rs146532042

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