RS797045993 MIR6857;SMC1A

Health Risk Chr X:53403617
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What This Variant Does
"CLNSIG=5
Associated Conditions
Congenital muscular hypertrophy-cerebral syndrome
SMC1A-related disorder
Congenital muscular hypertrophy-cerebral syndrome
SMC1A-related disorder
Other Variants in MIR6857;SMC1A
rs1569356550
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