ClinVar Miner

List of variants in gene TMC1 reported as benign for autosomal recessive nonsyndromic hearing loss 7

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 5
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HGVS dbSNP gnomAD frequency
NM_138691.3(TMC1):c.-219A>G rs7026304 0.55869
NM_138691.3(TMC1):c.-468G>A rs7022441 0.53167
NM_138691.3(TMC1):c.45C>T (p.Asp15=) rs2589615 0.51851
NM_138691.3(TMC1):c.241G>A (p.Glu81Lys) rs1796993 0.21988
NM_138691.3(TMC1):c.-329C>A rs7856724 0.13978

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