RS121909056 POU4F3

Health Risk Chr 5:146340292
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 15
Autosomal dominant nonsyndromic hearing loss 15
Other Variants in POU4F3
rs398124631 rs121909057 rs398123070 rs1064792854 rs759091617 rs759713394 rs149303333 rs766631025 rs1554087566 rs138310635
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