List of variants in gene SCLT1 reported as uncertain significance for perceptual disorders

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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: 8

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HGVS	dbSNP	gnomAD frequency
NM_144643.4(SCLT1):c.447A>T (p.Glu149Asp)	rs140181990	0.00066
NM_144643.4(SCLT1):c.1047+12A>G	rs770806266	0.00016
NM_144643.4(SCLT1):c.539A>G (p.Gln180Arg)	rs142407438	0.00011
NM_144643.4(SCLT1):c.367A>G (p.Ile123Val)	rs147766080	0.00002
NM_144643.4(SCLT1):c.130G>A (p.Asp44Asn)	rs149071636	0.00001
NM_144643.4(SCLT1):c.1613A>C (p.Gln538Pro)	rs759187846	0.00001
NM_144643.4(SCLT1):c.1046A>G (p.Gln349Arg)
NM_144643.4(SCLT1):c.2066A>T (p.Ter689Leu)	rs774832066

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