RS1247438528 SAMD9

Health Risk Chr 7:93103154
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Associated Conditions
Inborn genetic diseases
MIRAGE syndrome
Monosomy 7 myelodysplasia and leukemia syndrome 2
SAMD9-related disorder
Normophosphatemic familial tumoral calcinosis
Inborn genetic diseases
MIRAGE syndrome
Monosomy 7 myelodysplasia and leukemia syndrome 2
SAMD9-related disorder
Normophosphatemic familial tumoral calcinosis
Other Variants in SAMD9
rs121918554 rs767558735 rs1584254152 rs1584253343 rs1584251938 rs1064795431 rs1554337067 rs149966534 rs1554336981 rs572380130
Ask Dr. Hemsworth about this variant