ClinVar Miner

List of variants reported as benign for autosomal dominant nonsyndromic hearing loss 4A by Genome-Nilou Lab

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_001145809.2(MYH14):c.3033+11T>C rs930086 0.86981
NM_001145809.2(MYH14):c.5788-41A>G rs889002 0.83244
NM_001145809.2(MYH14):c.5678+12C>T rs3826772 0.78229
NM_001145809.2(MYH14):c.2694+30T>C rs1529492 0.74599
NM_001145809.2(MYH14):c.2250A>G (p.Pro750=) rs1651553 0.74436
NM_001145809.2(MYH14):c.5469+16C>T rs3745510 0.64922
NM_001145809.2(MYH14):c.5430G>A (p.Ser1810=) rs3745509 0.63924
NM_001145809.2(MYH14):c.657G>A (p.Ala219=) rs4801822 0.56915
NM_001145809.2(MYH14):c.3018G>A (p.Leu1006=) rs3745504 0.53291
NM_001145809.2(MYH14):c.3681-26A>T rs788337 0.50766
NM_001145809.2(MYH14):c.2355-14C>T rs12981413 0.46235
NM_001145809.2(MYH14):c.2205C>G (p.Arg735=) rs378811 0.38312
NM_001145809.2(MYH14):c.1114+13C>T rs11666328 0.32285
NM_001145809.2(MYH14):c.2355-17C>T rs28482851 0.23202
NM_001145809.2(MYH14):c.2827-9A>C rs3745503 0.14515

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