ClinVar Miner

List of variants in gene CLRN1 reported as benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP
NM_001195794.1(CLRN1):c.-71A>G rs3796240
NM_174878.3(CLRN1):c.*277_*278GT[13] rs34027634
NM_174878.3(CLRN1):c.*315C>T rs1456138
NM_174878.3(CLRN1):c.*372C>T rs4680058
NM_174878.3(CLRN1):c.*884A>C rs12635299
NM_174878.3(CLRN1):c.*964C>T rs16863066
NM_174878.3(CLRN1):c.254-1924T>A rs6764540
NM_174878.3(CLRN1):c.254-1947A>G rs6801898
NM_174878.3(CLRN1):c.254-2294A>C rs11914988
NM_174878.3(CLRN1):c.433+1105C>T rs16846663
NM_174878.3(CLRN1):c.57A>T (p.Ala19=) rs3796242
NM_174878.3(CLRN1):c.6A>C (p.Pro2=) rs111033422

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