RS1791543423 SAMD9

Health Risk Chr 7:93102220
Upload your DNA to see your genotype for this variant.
Associated Conditions
MIRAGE syndrome
Monosomy 7 myelodysplasia and leukemia syndrome 2
Normophosphatemic familial tumoral calcinosis
SAMD9-related disorder
MIRAGE syndrome
Monosomy 7 myelodysplasia and leukemia syndrome 2
Normophosphatemic familial tumoral calcinosis
SAMD9-related disorder
Other Variants in SAMD9
rs121918554 rs767558735 rs1584254152 rs1584253343 rs1584251938 rs1064795431 rs1554337067 rs149966534 rs1554336981 rs572380130
Ask Dr. Hemsworth about this variant