List of variants in gene CLRN1 reported as likely benign by Counsyl

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_174878.3(CLRN1):c.254-2132C>T	rs758741442	0.00003
NM_174878.3(CLRN1):c.254-2057T>C	rs778574679	0.00001
NM_174878.3(CLRN1):c.254-2082T>G	rs963890618	0.00001
NM_174878.3(CLRN1):c.254-2111del	rs1211060908	0.00001
NM_174878.3(CLRN1):c.336C>G (p.Thr112=)	rs565400473

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