RS118174674 LOXHD1

Health Risk Chr 18:46557436 snv missense variant

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Associated Conditions

Autosomal recessive nonsyndromic hearing loss 77

GWAS Studies (2)

Trait	Risk Allele	OR / Beta	P-value	Study
Age-related hearing impairment	T	OR: 3.65	2E-22	PubMed
Age-related hearing impairment (MTAG)	—	OR: 5.56	3E-8	PubMed

Population Frequencies

gnomAD ALL

98.2%

1kG AFR

0.1%

1kG ALL

0.7%

1kG AMR

98.3%

1kG EAS

100%

1kG EUR

97.7%

1kG SAS

100%

Other Variants in LOXHD1