ClinVar Miner

List of variants studied for autosomal recessive nonsyndromic hearing loss 3 by Hereditary Research Laboratory, Bethlehem University

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
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HGVS dbSNP gnomAD frequency
NM_016239.4(MYO15A):c.1223C>T (p.Ala408Val) rs191710555 0.00003
NM_016239.4(MYO15A):c.9572G>A (p.Arg3191His) rs373520843 0.00002
NM_016239.4(MYO15A):c.4240G>A (p.Glu1414Lys) rs1060499798
NM_016239.4(MYO15A):c.7207G>T (p.Asp2403Tyr) rs878853227

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