List of variants in gene WASHC5 reported as uncertain significance for Ritscher-Schinzel syndrome 1; Hereditary spastic paraplegia 8

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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_014846.4(WASHC5):c.2422A>G (p.Ile808Val)	rs144507279	0.00024
NM_014846.4(WASHC5):c.625G>A (p.Glu209Lys)	rs565980279	0.00002
NM_014846.4(WASHC5):c.872G>A (p.Ser291Asn)	rs753529606	0.00001

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