RS978197631 SAMD9
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Associated Conditions
Normophosphatemic familial tumoral calcinosis
Monosomy 7 myelodysplasia and leukemia syndrome 2
MIRAGE syndrome
Inborn genetic diseases
Normophosphatemic familial tumoral calcinosis
Monosomy 7 myelodysplasia and leukemia syndrome 2
MIRAGE syndrome
Inborn genetic diseases
Other Variants in SAMD9