ClinVar Miner

List of variants in gene CLRN1 reported as likely 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_174878.3(CLRN1):c.*1027T>G
NM_174878.3(CLRN1):c.*1191T>C
NM_174878.3(CLRN1):c.*1330T>C rs374292166
NM_174878.3(CLRN1):c.*277G>A rs200685524
NM_174878.3(CLRN1):c.254-2057T>C rs778574679
NM_174878.3(CLRN1):c.254-2082T>G rs963890618
NM_174878.3(CLRN1):c.254-2111del rs1211060908
NM_174878.3(CLRN1):c.254-2132C>T rs758741442
NM_174878.3(CLRN1):c.270C>G (p.Leu90=) rs143232961
NM_174878.3(CLRN1):c.336C>G (p.Thr112=) rs565400473
NM_174878.3(CLRN1):c.660C>T (p.Asp220=) rs148752352
NM_174878.3(CLRN1):c.9C>A (p.Ser3Arg) rs187218889

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