RS387906639 HARS1

Health Risk Chr 5:140674776
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What This Variant Does
"CLNSIG=5
Associated Conditions
Usher syndrome type 3B
Inborn genetic diseases
Usher syndrome type 3B
Inborn genetic diseases
Other Variants in HARS1
rs186526524 rs143473232 rs863225122 rs863225123 rs863225124 rs138582560 rs144588417 rs1239341211 rs147372931 rs78741041
Ask Dr. Hemsworth about this variant