RS749272546 LMBRD1

Health Risk Chr 6:69701470
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What This Variant Does
"CLNSIG=5
Associated Conditions
Inborn genetic diseases
Methylmalonic aciduria and homocystinuria type cblF
Cobalamin C disease
Disorders of Intracellular Cobalamin Metabolism
LMBRD1-related disorder
Inborn genetic diseases
Methylmalonic aciduria and homocystinuria type cblF
Cobalamin C disease
Disorders of Intracellular Cobalamin Metabolism
LMBRD1-related disorder
Other Variants in LMBRD1
rs779151199 rs1562112641 rs200639044 rs202207965 rs143642515 rs757392138 rs1380343985 rs534280770 rs747318789 rs1387756161
Ask Dr. Hemsworth about this variant