ClinVar Miner

List of variants studied for autosomal dominant nonsyndromic hearing loss 11 by Baylor Genetics

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
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HGVS dbSNP gnomAD frequency
NM_000260.4(MYO7A):c.6013A>G (p.Lys2005Glu) rs186644871 0.00031
NM_000260.4(MYO7A):c.6421A>G (p.Ile2141Val) rs761164010 0.00006
NM_000260.4(MYO7A):c.5510T>C (p.Leu1837Pro) rs1385324903 0.00001
NM_000260.4(MYO7A):c.2283-1G>T rs397516295
NM_000260.4(MYO7A):c.2573G>A (p.Arg858His) rs782428224
NM_000260.4(MYO7A):c.3226G>A (p.Glu1076Lys) rs1955328510
NM_000260.4(MYO7A):c.3560G>T (p.Ser1187Ile) rs1555090314

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