List of variants in gene IL11RA reported as likely pathogenic for bone development disease

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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_001142784.3(IL11RA):c.781C>T (p.Arg261Cys)	rs201638429	0.00005
NM_001142784.3(IL11RA):c.810G>A (p.Thr270=)	rs1258408605	0.00003
NM_001142784.3(IL11RA):c.281G>T (p.Cys94Phe)	rs369630361	0.00002
NM_001142784.3(IL11RA):c.662C>G (p.Pro221Arg)	rs387906785	0.00001

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