List of variants in gene HLCS reported as benign 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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001352514.2(HLCS):c.1893-46G>T	rs2073421	0.59296
NM_001352514.2(HLCS):c.1438-36G>A	rs2073425	0.55169
NM_001352514.2(HLCS):c.2122-30G>A	rs2073420	0.40931
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.1960+16T>A	rs73398135	0.03462
NM_001352514.2(HLCS):c.2361C>T (p.Val787=)	rs61732507	0.02015
NM_001352514.2(HLCS):c.1494C>T (p.Asn498=)	rs1065759	0.01068
NM_000411.8(HLCS):c.-393+9391A>G	rs112242941	0.00866
NM_001352514.2(HLCS):c.1412G>A (p.Arg471His)	rs61732501	0.00850
NM_001352514.2(HLCS):c.494-13A>G	rs76785742	0.00759
NM_001352514.2(HLCS):c.726C>T (p.Pro242=)	rs2230182	0.00587
NM_001352514.2(HLCS):c.331-7157C>T	rs149104163	0.00524
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.2451-19C>T	rs78671947	0.00290
NM_001352514.2(HLCS):c.*19C>T	rs137949852	0.00259
NM_001352514.2(HLCS):c.2121+11T>A	rs371974889	0.00105
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.7_9del	rs201681436
NM_001352514.2(HLCS):c.1620+7del	rs140568778
NM_001352514.2(HLCS):c.1621-13_1621-10del	rs377641674

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