RS369698072 NBAS
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Short stature-optic atrophy-Pelger-Huët anomaly syndrome
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Short stature-optic atrophy-Pelger-Huët anomaly syndrome
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins
Other Variants in NBAS