ClinVar Miner

List of variants studied for autosomal recessive nonsyndromic hearing loss 22 by Genome-Nilou Lab

Included ClinVar conditions (1):

Autosomal recessive nonsyndromic hearing loss 22

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Minimum conflict level: Report conflict between different conditions
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Total variants: 5

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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.2302-26C>T	rs56065183

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