ClinVar Miner

List of variants studied for autosomal recessive nonsyndromic hearing loss 22 by Baylor Genetics

Included ClinVar conditions (1):

Autosomal recessive nonsyndromic hearing loss 22

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Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_144672.4(OTOA):c.268-677G>A	rs931046043	0.00007
NM_144672.4(OTOA):c.1049T>C (p.Leu350Pro)
NM_144672.4(OTOA):c.1912C>T (p.Gln638Ter)	rs1898923522
NM_144672.4(OTOA):c.2352del (p.Thr785fs)

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