List of variants in gene FAM20A reported as uncertain significance 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_017565.4(FAM20A):c.467G>A (p.Arg156Gln)	rs146809464	0.00033
NM_017565.4(FAM20A):c.440C>T (p.Thr147Ile)	rs145784842	0.00023
NM_017565.4(FAM20A):c.527G>A (p.Arg176Gln)	rs140917285	0.00019
NM_017565.4(FAM20A):c.5C>T (p.Pro2Leu)	rs528874230	0.00014
NM_017565.4(FAM20A):c.13C>A (p.Arg5Ser)	rs766476867	0.00004
NM_017565.4(FAM20A):c.53T>A (p.Leu18Gln)

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