List of variants in gene ALMS1 reported as uncertain significance for retinal disorder

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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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001378454.1(ALMS1):c.7846C>T (p.Arg2616Trp)	rs145383239	0.00006
NM_001378454.1(ALMS1):c.10538A>T (p.Asp3513Val)	rs767343226	0.00001
NM_001378454.1(ALMS1):c.5538G>T (p.Leu1846=)	rs768057574	0.00001
NM_001378454.1(ALMS1):c.1135A>G (p.Asn379Asp)	rs1671347836

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