List of variants reported as uncertain significance for Revesz syndrome; Dyskeratosis congenita, autosomal dominant 1; Dyskeratosis congenita, autosomal dominant 3

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001099274.3(TINF2):c.403C>T (p.Leu135Phe)	rs199740488	0.00012
NM_001099274.3(TINF2):c.936C>A (p.Tyr312Ter)	rs201677741	0.00006
NM_001099274.3(TINF2):c.802G>C (p.Val268Leu)	rs369926102	0.00001
NM_001099274.3(TINF2):c.1285C>A (p.Leu429Ile)	rs780647966

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