List of variants in gene TNFRSF1A reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001065.4(TNFRSF1A):c.236C>T (p.Thr79Met)	rs104895219
NM_001065.4(TNFRSF1A):c.295T>C (p.Cys99Arg)	rs104895228
NM_001065.4(TNFRSF1A):c.596T>A (p.Ile199Asn)	rs104895247

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