RS148653339 NEFH

Health Risk Chr 22:29485808
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Associated Conditions
Inborn genetic diseases
NEFH-related disorder
Amyotrophic lateral sclerosis type 1
Charcot-Marie-Tooth disease axonal type 2CC
Inborn genetic diseases
NEFH-related disorder
Amyotrophic lateral sclerosis type 1
Charcot-Marie-Tooth disease axonal type 2CC
Other Variants in NEFH
rs606231212 rs267607534 rs59551486 rs61556467 rs139580489 rs876657411 rs876657412 rs1602961831 rs780966618 rs776050286
Ask Dr. Hemsworth about this variant