RS387907017 ILDR1

Health Risk Chr 3:122001371
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What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive nonsyndromic hearing loss 42
Rare genetic deafness
Autosomal recessive nonsyndromic hearing loss 42
Rare genetic deafness
Other Variants in ILDR1
rs387907015 rs387907016 rs141559449 rs150250182 rs142746163 rs143072070 rs369318229 rs186672543 rs201105694 rs746732835
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