RS104893977 NEU1

Health Risk Chr 6:31860458
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What This Variant Does
"[OMIM:?]
Associated Conditions
Sialidosis type 2
Autosomal recessive NEU1-related disorders
Sialidosis type 2
Autosomal recessive NEU1-related disorders
Other Variants in NEU1
rs104893971 rs104893972 rs1301852124 rs193922915 rs1581820081 rs28940583 rs104893983 rs104893984 rs104893985 rs104893978
Ask Dr. Hemsworth about this variant