ClinVar Miner

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

Included ClinVar conditions (311):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
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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