RS370712489 POU4F3

Health Risk Chr 5:146339641
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Associated Conditions
Autosomal dominant nonsyndromic hearing loss 15
Hearing impairment
Inborn genetic diseases
Autosomal dominant nonsyndromic hearing loss 15
Hearing impairment
Inborn genetic diseases
Other Variants in POU4F3
rs398124631 rs121909056 rs121909057 rs398123070 rs1064792854 rs759091617 rs759713394 rs149303333 rs766631025 rs1554087566
Ask Dr. Hemsworth about this variant