List of variants in gene HLCS reported as benign by PreventionGenetics, part of Exact Sciences

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: 8

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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.1893-6C>T	rs139904712	0.00313
NM_001352514.2(HLCS):c.865G>A (p.Val289Ile)	rs149291867	0.00087

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