List of variants in gene MIR6857, SMC1A studied for multiple congenital anomalies/dysmorphic syndrome

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_006306.4(SMC1A):c.1732-19A>G	rs2146599868
NM_006306.4(SMC1A):c.1732-6C>T
NM_006306.4(SMC1A):c.1732-7C>A
NM_006306.4(SMC1A):c.2420G>A (p.Arg807His)	rs1569356550

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