List of variants in gene combination LOC129930352, P3H1 reported as likely benign for bone development 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_022356.4(P3H1):c.207C>T (p.Arg69=)	rs900120741	0.00002
NM_022356.4(P3H1):c.210C>T (p.Ala70=)	rs756652599	0.00001
NM_022356.4(P3H1):c.219G>C (p.Leu73=)	rs191472592	0.00001
NM_022356.4(P3H1):c.217C>T (p.Leu73=)
NM_022356.4(P3H1):c.297G>A (p.Ser99=)
NM_022356.4(P3H1):c.297G>C (p.Ser99=)

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