RS202162088 SAMD9L
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Associated Conditions
Spinocerebellar ataxia 49
Monosomy 7 myelodysplasia and leukemia syndrome 1
Ataxia-pancytopenia syndrome
Inborn genetic diseases
Spinocerebellar ataxia 49
Monosomy 7 myelodysplasia and leukemia syndrome 1
Ataxia-pancytopenia syndrome
Inborn genetic diseases
Other Variants in SAMD9L