RS587784412 SMC1A

Health Risk Chr X:53403618
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital muscular hypertrophy-cerebral syndrome
Inborn genetic diseases
Microcephaly
Congenital muscular hypertrophy-cerebral syndrome
Inborn genetic diseases
Microcephaly
Other Variants in SMC1A
rs1602407457 rs122454122 rs2520970863 rs122454123 rs387906702 rs112727682 rs587784419 rs587784418 rs587784417 rs587784416
Ask Dr. Hemsworth about this variant