RS121912947 COL11A2

Health Risk Chr 6:33171763
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What This Variant Does
"[OMIM:?]
Associated Conditions
Autosomal dominant nonsyndromic hearing loss 13
Rare genetic deafness
COL11A2-related disorder
Autosomal dominant nonsyndromic hearing loss 13
Rare genetic deafness
COL11A2-related disorder
Other Variants in COL11A2
rs750995470 rs121912945 rs864309477 rs121912946 rs121912948 rs121912949 rs121912950 rs121912951 rs121912952 rs1562315748
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