RS80338760 SEPTIN9

Health Risk Chr 17:77320193
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What This Variant Does
"A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in ...
Associated Conditions
Amyotrophic neuralgia
Amyotrophic neuralgia
Other Variants in SEPTIN9
rs80338761 rs80338762 rs769442066 rs199861986 rs201560726 rs544797046 rs200031107 rs886053495 rs539303139 rs763954299
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