List of variants in gene DVL1 reported as likely 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001330311.2(DVL1):c.1366A>G (p.Thr456Ala)	rs140107023	0.00213
NM_001330311.2(DVL1):c.272C>T (p.Ala91Val)	rs145496306	0.00210
NM_001330311.2(DVL1):c.1502G>C (p.Cys501Ser)	rs139708222	0.00055
NM_001330311.2(DVL1):c.1136C>T (p.Thr379Met)	rs755390263	0.00003
NM_001330311.2(DVL1):c.584A>G (p.Asp195Gly)	rs758508750	0.00001
NM_001330311.2(DVL1):c.1163G>C (p.Arg388Pro)
NM_001330311.2(DVL1):c.1398G>T (p.Glu466Asp)	rs2100718483

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