List of variants in gene RPL13 reported as likely pathogenic for bone 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_000977.4(RPL13):c.477+1G>A	rs1597675888
NM_000977.4(RPL13):c.516dup (p.Glu173fs)
NM_000977.4(RPL13):c.548G>A (p.Arg183His)	rs1597676540
NM_000977.4(RPL13):c.569G>T (p.Arg190Leu)	rs374646539

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