List of variants in gene SMS reported as uncertain significance for Syndromic X-linked intellectual disability Snyder type

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_004595.5(SMS):c.1019A>G (p.Glu340Gly)	rs751460863	0.00002
NM_004595.5(SMS):c.799G>A (p.Gly267Arg)	rs757074790	0.00002
NM_004595.5(SMS):c.872C>A (p.Thr291Lys)	rs755701744	0.00001
NM_004595.5(SMS):c.997G>C (p.Gly333Arg)	rs1200431087	0.00001
NM_004595.5(SMS):c.1061+2T>C
NM_004595.5(SMS):c.113C>T (p.Ser38Leu)
NM_004595.5(SMS):c.170+3G>C
NM_004595.5(SMS):c.261C>G (p.Asp87Glu)
NM_004595.5(SMS):c.289A>G (p.Met97Val)
NM_004595.5(SMS):c.329G>A (p.Arg110Gln)	rs2147513193
NM_004595.5(SMS):c.641_643del (p.Lys214del)

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