List of variants in gene CLRN1 reported as benign for autosomal recessive disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_174878.3(CLRN1):c.254-1924T>A	rs6764540	0.79708
NM_174878.3(CLRN1):c.*315C>T	rs1456138	0.76689
NM_174878.3(CLRN1):c.*372C>T	rs4680058	0.76596
NM_174878.3(CLRN1):c.254-1947A>G	rs6801898	0.54588
NM_001195794.1(CLRN1):c.-71A>G	rs3796240	0.48434
NM_174878.3(CLRN1):c.254-2294A>C	rs11914988	0.20293
NM_174878.3(CLRN1):c.57A>T (p.Ala19=)	rs3796242	0.12205
NM_174878.3(CLRN1):c.*884A>C	rs12635299	0.08952
NM_174878.3(CLRN1):c.*964C>T	rs16863066	0.03941
NM_174878.3(CLRN1):c.6A>C (p.Pro2=)	rs111033422	0.03830
NM_174878.3(CLRN1):c.433+1105C>T	rs16846663	0.03733
NM_174878.3(CLRN1):c.*277GT[13]	rs34027634

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