RS779584313 SEPTIN9

Health Risk Chr 17:77402601
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Associated Conditions
Inborn genetic diseases
Amyotrophic neuralgia
Inborn genetic diseases
Amyotrophic neuralgia
Other Variants in SEPTIN9
rs80338761 rs80338762 rs80338760 rs769442066 rs199861986 rs201560726 rs544797046 rs200031107 rs886053495 rs539303139
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