List of variants in gene RLIM reported as pathogenic for X-linked 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_016120.4(RLIM):c.1067A>G (p.Tyr356Cys)	rs786205133
NM_016120.4(RLIM):c.1093C>T (p.Arg365Cys)	rs1569309816
NM_016120.4(RLIM):c.1159C>T (p.Arg387Cys)	rs1569309776
NM_016120.4(RLIM):c.1760C>G (p.Pro587Arg)	rs1569309474
NM_016120.4(RLIM):c.1792G>A (p.Asp598Asn)	rs1569309460
NM_016120.4(RLIM):c.1795C>T (p.Arg599Cys)	rs1569309459
NM_016120.4(RLIM):c.1831C>T (p.Arg611Cys)	rs1569309449

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