ClinVar Miner

List of variants reported as benign for autosomal recessive nonsyndromic hearing loss 22

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 9
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HGVS dbSNP gnomAD frequency
NM_144672.4(OTOA):c.1630-5C>T rs215901 0.62768
NM_144672.4(OTOA):c.*47A>G rs460598 0.37728
NM_144672.4(OTOA):c.3056-23C>T rs201448090 0.23237
NM_144672.4(OTOA):c.179+27G>A rs12445216 0.19188
NM_144672.4(OTOA):c.2229C>T (p.Ala743=) rs461179 0.03046
NM_144672.4(OTOA):c.2238G>A (p.Thr746=) rs72640475 0.01270
NM_144672.4(OTOA):c.1105-17G>A rs73549643 0.01254
NM_144672.4(OTOA):c.121-20G>A rs7187792 0.00516
NM_144672.4(OTOA):c.2302-26C>T rs56065183

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