List of variants in gene TRPV6 reported as uncertain significance 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_018646.6(TRPV6):c.614A>G (p.His205Arg)	rs200186434	0.00013
NM_018646.6(TRPV6):c.1969G>A (p.Gly657Arg)	rs576385529	0.00002
NM_018646.6(TRPV6):c.1744G>A (p.Asp582Asn)	rs745903672
NM_018646.6(TRPV6):c.524C>T (p.Ala175Val)	rs1795093724
NM_018646.6(TRPV6):c.713C>G (p.Thr238Arg)	rs1795077287
NM_018646.6(TRPV6):c.970G>A (p.Asp324Asn)	rs757050801

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