RS80338761 SEPTIN9

Health Risk Chr 17:77402298
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What This Variant Does
"[OMIM:?]
Associated Conditions
Amyotrophic neuralgia
Inborn genetic diseases
Amyotrophic neuralgia
Inborn genetic diseases
Other Variants in SEPTIN9
rs80338762 rs80338760 rs769442066 rs199861986 rs201560726 rs544797046 rs200031107 rs886053495 rs539303139 rs763954299
Ask Dr. Hemsworth about this variant