List of variants in gene RLIM reported as uncertain significance for Intellectual disability, X-linked 61

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_016120.4(RLIM):c.1358G>A (p.Ser453Asn)	rs201787580	0.00003
NM_016120.4(RLIM):c.507A>C (p.Glu169Asp)	rs1285137481	0.00002
NM_016120.4(RLIM):c.1115G>A (p.Arg372Gln)	rs764084971	0.00001
NM_016120.4(RLIM):c.1490A>G (p.Asn497Ser)	rs2147371855	0.00001
NM_016120.4(RLIM):c.1045A>G (p.Thr349Ala)
NM_016120.4(RLIM):c.1311G>A (p.Met437Ile)	rs2079618376
NM_016120.4(RLIM):c.131A>G (p.Tyr44Cys)	rs2519837398
NM_016120.4(RLIM):c.1364C>A (p.Ser455Tyr)	rs1478259309
NM_016120.4(RLIM):c.1401_1412del (p.Ser473_Ser476del)	rs749149244
NM_016120.4(RLIM):c.1508C>T (p.Ser503Leu)	rs2519833766
NM_016120.4(RLIM):c.1529G>A (p.Arg510Gln)
NM_016120.4(RLIM):c.736A>G (p.Ile246Val)	rs2079620974
NM_016120.4(RLIM):c.74G>T (p.Arg25Leu)	rs2079637855
NM_016120.4(RLIM):c.826T>C (p.Ser276Pro)	rs768846788

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