List of variants in gene RELT reported as pathogenic for dental enamel hypoplasia

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_152222.2(RELT):c.1264C>T (p.Arg422Trp)	rs139368769	0.00108
NM_152222.2(RELT):c.1169_1170del (p.Pro390fs)	rs772929908	0.00004
NM_152222.2(RELT):c.121-2A>G	rs1565222166
NM_152222.2(RELT):c.1265G>C (p.Arg422Pro)	rs762816338
NM_152222.2(RELT):c.164C>T (p.Thr55Ile)	rs1866200282

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