List of variants reported as likely benign for Congenital muscular hypertrophy-cerebral syndrome

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Total variants: 16

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HGVS	dbSNP
NM_001281463.1(SMC1A):c.-150C>T	rs781999328
NM_001281463.1(SMC1A):c.1032G>A (p.Thr344=)	rs140585416
NM_001281463.1(SMC1A):c.2884G>A (p.Gly962Ser)	rs782381563
NM_001281463.1(SMC1A):c.3525C>T (p.Ala1175=)	rs146216425
NM_001281463.1(SMC1A):c.3552+7C>T	rs782267492
NM_001281463.1(SMC1A):c.3597C>T (p.Thr1199=)	rs28997583
NM_006306.4(SMC1A):c.*3087G>A
NM_006306.4(SMC1A):c.1863C>T (p.Asn621=)	rs782665597
NM_006306.4(SMC1A):c.2039G>A (p.Arg680His)	rs1556889522
NM_006306.4(SMC1A):c.2556C>A (p.Leu852=)	rs1602407405
NM_006306.4(SMC1A):c.3063C>T (p.Ala1021=)	rs202083908
NM_006306.4(SMC1A):c.3177C>T (p.Phe1059=)	rs375312256
NM_006306.4(SMC1A):c.3205C>T (p.Arg1069Cys)
NM_006306.4(SMC1A):c.3286-4C>T	rs1556885985
NM_006306.4(SMC1A):c.579G>A (p.Ala193=)	rs199571320
NM_006306.4(SMC1A):c.764G>A (p.Arg255His)

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