List of variants in gene SMARCAD1 reported as benign for Keratoderma with scleroatrophy of the extremities

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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_020159.5(SMARCAD1):c.902T>C (p.Val301Ala)	rs7439869	0.69652
NM_020159.5(SMARCAD1):c.1839C>T (p.Asp613=)	rs6823404	0.52569
NM_020159.5(SMARCAD1):c.1479A>G (p.Gln493=)	rs2306802	0.38873
NM_020159.5(SMARCAD1):c.740G>A (p.Ser247Asn)	rs11722476	0.36530

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