List of variants in gene TRPV4 reported as not provided by GenomeConnect - Invitae Patient Insights Network

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_021625.5(TRPV4):c.37G>T (p.Gly13Trp)	rs763302555	0.00003
NM_021625.5(TRPV4):c.686C>T (p.Ser229Leu)	rs373980330	0.00001
NM_021625.5(TRPV4):c.2246C>G (p.Pro749Arg)	rs1555205050

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