List of variants in gene FAM20A reported as likely benign for tooth hard tissue disease

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_017565.4(FAM20A):c.640+11T>C	rs8071830	0.02884
NM_017565.4(FAM20A):c.18G>A (p.Arg6=)	rs75228334	0.01179
NM_017565.4(FAM20A):c.513T>C (p.His171=)	rs181817943	0.00030
NM_017565.4(FAM20A):c.43C>T (p.Leu15=)	rs372862593	0.00020
NM_017565.4(FAM20A):c.404+18G>A	rs773191671	0.00011
NM_017565.4(FAM20A):c.321G>C (p.Pro107=)	rs568029338	0.00007
NM_017565.4(FAM20A):c.342C>T (p.Asp114=)	rs778101746	0.00006
NM_017565.4(FAM20A):c.195C>T (p.Gly65=)

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