List of variants in gene FAM20C reported as benign for bone disorder

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_020223.4(FAM20C):c.1254-63T>C	rs36164325	0.61141
NM_020223.4(FAM20C):c.956+61A>G	rs146778412	0.55843
NM_020223.4(FAM20C):c.*41C>G	rs36138803	0.53518
NM_020223.4(FAM20C):c.1659G>T (p.Val553=)	rs36170987	0.52970
NM_020223.4(FAM20C):c.1363+10G>A	rs36156504	0.30098
NM_020223.4(FAM20C):c.885A>G (p.Thr295=)	rs141256626	0.29810
NM_020223.4(FAM20C):c.*30G>A	rs36173075	0.25167
NM_020223.4(FAM20C):c.1749G>A (p.Ala583=)	rs143027699	0.06313
NM_020223.4(FAM20C):c.1072+23A>G	rs185225273	0.04519
NM_020223.4(FAM20C):c.1740C>T (p.Ala580=)	rs563226142	0.00273
NM_020223.4(FAM20C):c.1506-55G>A	rs36156024
NM_020223.4(FAM20C):c.1690A>G (p.Asn564Asp)	rs36139924
NM_020223.4(FAM20C):c.953_956+30dup	rs771282640

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