List of variants in gene SMS reported as likely pathogenic for syndromic intellectual disability

Minimum submission review status:		Collection method:
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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_004595.5(SMS):c.152A>G (p.Tyr51Cys)	rs2147508108
NM_004595.5(SMS):c.328C>G (p.Arg110Gly)	rs1924243873
NM_004595.5(SMS):c.335C>A (p.Pro112Gln)
NM_004595.5(SMS):c.410A>G (p.Asp137Gly)	rs1924586809
NM_004595.5(SMS):c.581T>G (p.Val194Gly)
NM_004595.5(SMS):c.587T>C (p.Ile196Thr)	rs1924648986
NM_004595.5(SMS):c.674T>C (p.Val225Ala)
NM_004595.5(SMS):c.700C>T (p.Arg234Ter)
NM_004595.5(SMS):c.865+2T>C	rs2146953457

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