ClinVar Miner

List of variants in gene TNFRSF1A reported as likely pathogenic for Inborn genetic diseases

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Gene type:
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Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_001065.4(TNFRSF1A):c.123T>G (p.Asp41Glu) rs104895271
NM_001065.4(TNFRSF1A):c.184T>G (p.Cys62Gly) rs104895225
NM_001065.4(TNFRSF1A):c.250T>C (p.Cys84Arg) rs104895253

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