List of variants in gene TRPV4 reported as benign by Molecular Genetics Laboratory, London Health Sciences Centre

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_021625.5(TRPV4):c.670A>C (p.Arg224=)	rs3825394	0.60669
NM_021625.5(TRPV4):c.2034C>T (p.Ile678=)	rs3742037	0.14446
NM_021625.5(TRPV4):c.789T>C (p.Asp263=)	rs3742034	0.12664
NM_021625.5(TRPV4):c.795C>T (p.His265=)	rs1344554	0.08478
NM_021625.5(TRPV4):c.55C>T (p.Pro19Ser)	rs3742030	0.03470
NM_021625.5(TRPV4):c.2459-9T>G	rs115373018	0.02700
NM_021625.5(TRPV4):c.81T>C (p.Gly27=)	rs34599967	0.02557
NM_021625.5(TRPV4):c.854-5C>T	rs116401333	0.02337
NM_021625.5(TRPV4):c.387-4C>T	rs12305439	0.01630
NM_021625.5(TRPV4):c.33G>T (p.Gly11=)	rs56092423	0.00939
NM_021625.5(TRPV4):c.1684G>A (p.Val562Ile)	rs56177950	0.00760
NM_021625.5(TRPV4):c.2518G>A (p.Glu840Lys)	rs55728855	0.00718
NM_021625.5(TRPV4):c.2433G>C (p.Ser811=)	rs34071623	0.00673
NM_021625.5(TRPV4):c.810G>A (p.Gly270=)	rs147558344	0.00582
NM_021625.5(TRPV4):c.1153-10C>T	rs149541389	0.00547
NM_021625.5(TRPV4):c.1744C>T (p.Leu582=)	rs35078611	0.00542
NM_021625.5(TRPV4):c.1713C>G (p.Ile571Met)	rs185933892	0.00191
NM_021625.5(TRPV4):c.649G>T (p.Ala217Ser)	rs187864727	0.00172
NM_021625.5(TRPV4):c.57C>T (p.Pro19=)	rs112408790	0.00161
NM_021625.5(TRPV4):c.1585-18C>T	rs201974634	0.00148
NM_021625.5(TRPV4):c.1333-16A>C	rs199994834
NM_021625.5(TRPV4):c.1584+18G>C	rs10850750
NM_021625.5(TRPV4):c.396G>A (p.Pro132=)	rs114101785

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