RS121912560 MYO6

Health Risk Chr 6:75841299

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What This Variant Does

"[OMIM:?]

Associated Conditions

Rare genetic deafness

Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome

Rare genetic deafness

Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome

GWAS Studies (8)

Trait	Risk Allele	OR / Beta	P-value	Study
Hearing loss	—	OR: 30.67	3E-15	PubMed
Hearing aid use	G	OR: 5.28	5E-14	PubMed
Hearing difficulty and hearing difficulty with background noise	G	OR: 3.86	9E-13	PubMed
Hearing difficulty	G	OR: 3.73	2E-12	PubMed
Hearing aid use	G	OR: 5.48	2E-10	PubMed
Hearing difficulty and hearing difficulty with background noise	G	OR: 3.73	4E-10	PubMed
Hearing difficulty with background noise	G	OR: 3.26	1E-9	PubMed
Hearing difficulty	G	OR: 3.54	3E-9	PubMed

Other Variants in MYO6